DCCC

DC Cancer Plan
Table of Contents
  1. Statement of Support for the DC Cancer Plan
  2. Executive Summary
  3. Goals and Objectives
  4. Introduction
  5. Access to Care
  6. Cancer Prevention
  7. Smoking-Related Cancers
  8. Head and Neck Cancers
  9. Breast Cancer
  10. Gynecologic Cancers
  11. Colorectal Cancer
  12. Prostate Cancer
  13. Pediatric Cancers
  14. Palliative Care
  15. Cancer Survivorship
  16. Cancer Rehabilitation
  17. Putting the Plan into Action
  18. American Cancer Society Screening Guidelines
  19. Contributors


Statement of Support for
the DC Cancer Plan

            As the directors of the District of Columbia ’s major cancer research and treatment centers, we see the consequences of cancer in our community every day.

            As much as the cancer centers and cancer-related organizations in the District work to reduce the number of people being diagnosed with, suffering from, and dying from cancer, we realize that much more is needed. The Cancer Plan before you provides a blueprint for the next steps to be taken if we are to make meaningful progress toward reducing suffering and death from cancer.

            We must work together if we are to reduce the burden of cancer in our city. To that end, the DC Cancer Coalition, a broad partnership of public and private institutions, organizations, and advocates has developed a comprehensive, coordinated plan with specific strategies to have a greater impact on cancer in the District. Our institutions are committed to work collaboratively together and with the cancer community in implementing the Plan, and we invite all other concerned citizens and organizations to join us.

Please become familiar with the Plan. Talk with your colleagues. Then identify how your institution, agency, or organization can use the Plan as a guide for your own activities and consider what role you can play in implementing strategies for the greater good of the citizens of the District of Columbia . In the days ahead, leaders of the Cancer Plan will reach out to you and seek your ideas, insight, and assistance. We hope you will respond. The lives of many citizens in our community depend on the efforts of all of us.

 

Lucile Adams-Campbell, PhD                                          Steven Patierno, PhD
Director, Howard University Cancer Center                       Executive Director, The George Washington
Howard University                                                          University Cancer Institute
                                                                                    The George Washington University

 

   

Lawrence S. Lessin, MD                                     Richard G. Pestell, MD, PhD
Medical Director, Washington Cancer Institute                  Director, Lombardi Comprehensive Cancer
Washington Hospital Center                                             Center
                                                                                    Georgetown University

 

      <top>


Executive Summary:
The Face of Cancer in the District of Columbia
      <top>


Creating the District’s First Cancer Plan

In 2001, because the District of Columbia has the highest cancer mortality rate in the United States , the DC Department of Health (DOH) created the DC Cancer Control Coalition to serve as a partner in addressing
comprehensive cancer control and prevention. In 2003, the Department of Health received initial funding from the Centers for Disease Control and Prevention to begin this process.

The Coalition is a partnership of medical centers, nonprofit organizations, academic and research institutions, community groups, advocates, professional organizations, and others. We have worked together for four years to produce the District’s first Cancer Plan—an analysis of the present environment, a blueprint to reduce the number of new cases of cancer and the number of cancer-caused deaths and to improve the quality of life for cancer survivors in the nation’s capital.

As you will see, the need is urgent.

Cancer in the District: Portrait of Inequity

Our city of 560,178 residents—the nation’s capital—has the highest cancer mortality rate per population in the United States . In 2005, according to American Cancer Society
projections, about 2,820 individuals will be
diagnosed with cancer in the District, and 1,170 will die of the disease. Cancer is the leading cause of death in DC among those 85 years and younger.

These high rates exist despite having four cancer centers, a total of 11 hospitals, and an abundance of excellent cancer care services. But many of these services are neither accessible nor affordable for many of DC’s citizens—the poor and medically underserved (uninsured and underinsured), most of whom are Black or Hispanic.
Inequitable distribution of cancer care plays a major role in the city’s high mortality rates, and in every aspect of cancer control: screening, early detection, treatment, survivorship, palliative and end-of-life care.

About 58% of the District’s population is Black, 27% is White and 3% Asian. About 10% of the population is of Hispanic origin (some self-identifying as White, and some as Black). Another 2% describe themselves as “two or more races or other.” [Thomson Medstat©2004] The Hispanic population is the city’s fastest-growing and includes many of the poorest residents. Hispanic residents are the least likely to have health insurance of any kind.

Key factors influencing the high rates of cancer incidence and mortality include

Lack of medical homes. Many of the District’s residents—about 300,000—live in a “Health Professional Shortage Area (HPSA).” This includes many of the working poor. These residents lack what is called a “medical home,” a primary care provider who knows their health history and is a reliable source of routine medical care. The single largest determining factor in the use of cancer services, from prevention through treatment and follow-up, is having a primary care physician who makes recommendations and provides assistance in navigating the health care system. The DC Primary Care Association (DCPCA) links this lack of adequate primary care to poorer health outcomes, higher health care costs, and   overused, overcrowded emergency rooms. “Because people can’t find a doctor,”
explains DCPCA, “they delay care, escalating the severity of illness to crisis and contributing to high disability rates.”

Screening difficulties. Deaths from breast, cervical, colorectal, and prostate cancer can be avoided or decreased through screening procedures. However, facilities for cancer screening are few and far between in the District’s poorer neighborhoods. Most screening resources are located north of the Anacostia River , and many of the District’s poorest neighborhoods, where many of the cancer deaths occur, are southeast of the river. Remote locations for screening present a formidable barrier to participation.

Additionally, the District underfunds
screening programs for breast and cervical cancer. Project WISH, a CDC-funded screening program for breast and cervical cancers, has been hampered by problems related to management, reimbursement of providers, tracking, and patient follow-up.
At this time, there is also no District funding allocated, and there are no systemic programs for, prostate and colorectal cancer screening.

The health care labyrinth. In addition to its many hospitals and medical centers, the District prides itself on having many public and private health care clinics. However, the clinics are only loosely linked to each other and to other parts of the health care system. It can take people with symptoms a long time to get a clinic appointment, and a patient who does manage to get screened and receives a screening result indicating possible cancer may not get appropriate
follow-up care, medications, counseling, rehabilitation and services like transportation.

It can be very difficult for any patient—rich or poor, highly educated or uneducated—
to navigate through the health care labyrinth in the District. When a diagnosis of cancer is compounded by factors such as limited English proficiency, poverty, cultural
or cognitive barriers, lack of reliable transportation, and considerable distances to travel for care, it is not difficult to understand that people become overwhelmed and may elect to drop out of all or part of the health care system that exists, and not complete cancer treatments.

Information deficit. The DC Cancer
Registry has had difficulty collecting sufficient data on cancer in the Hispanic community, despite the fact that this segment is the City’s fastest-growing population. This data is needed to design effective measures for cancer control in the Hispanic community.

Fragmented health insurance system. The DC HealthCare Alliance, in partnership with the DC Department of Health, private and nonprofit health clinics, offers low-income residents access to an array of health care services. Because the Alliance is extremely underfunded, it has never enrolled all eligible people. Specialists often avoid participating in its network because the Alliance reimburses physicians and hospitals very slowly and far below the actual cost of care (15 cents on the dollar). Hospitals and physicians who serve Alliance or Medicaid patients in the emergency room are not reimbursed at all. The District’s hospitals annually must absorb millions of dollars of uncompensated care—so much that some hospitals now are refusing to treat Alliance patients. This is clearly a broken system that fails to serve DC’s neediest patients with an array of illnesses—not only cancer—and meaningful reform is urgently needed.

  The Department of Health reports that a number of steps have been taken to further integrate and improve the Alliance and Medicaid, including appointment of a single Medical Director, adoption of HEDIS (Health Plan Employer Data and Information Set) measure reporting, implementation of new waivers, use of managed care organizations, and dual use of Income Management Administration. The DOH further notes that the department is in the midst of a major reform of the DC Alliance that will take effect in 2006.

It should be noted that, unlike most states, the District of Columbia fails to spend any tobacco settlement funds received on health care and cancer services. This has left the city with almost no infrastructure with which to build an effective cancer control and prevention program.

The bottom line is that many of the District’s neediest residents cannot or do not take advantage of available cancer care in the District. They struggle to navigate the convoluted health care system, the programs designed to provide care often fail to do so, there is no substantive public health structure—and as a result people are dying of cancer at high rates, despite living near highly sophisticated cancer care facilities.

Plan preparation and components

The DC Cancer Coalition workgroups (including physicians, public health experts, community leaders and others) have developed specific research-based chapters of the Plan. In each chapter, we assess the cancer burden, address current resources, identify gaps in care, and set forth prioritized recommendations that we believe will set the District and the health care community on course to correct the problems presented.

 In the chapters that follow, we present separate discussions, goals, objectives and strategies for the following areas: Access to Care, Cancer Prevention, Smoking-Related Cancers, Head and Neck Cancers, Breast Cancer, Gynecologic Cancers, Colorectal Cancer, Prostate Cancer, Pediatric Cancers, Palliative Care, Cancer Survivorship, and Cancer Rehabilitation. In a separate document, we will also publish a resource guide for the region, The Community Resource Directory for Cancer Survivors and Caregivers.

What Must Be Done: Implementation

The next step in addressing cancer control and prevention is to use the Cancer Plan to move the District forward. We understand that bringing the Cancer Plan to life is the work of years, and that with individual and collaborative actions must come ongoing evaluation and mid-course corrections as needed to respond to the changing
environment around us. At every step of the way, it will remain important to seek input from stakeholders throughout the city on progress and problems.

Some of the work ahead will require examining public policy that affects cancer in DC. Other priorities demand new avenues of collaboration among the city’s health care providers, and securing the funding necessary to make collaboration possible and effective. These tasks are formidable, but the Coalition’s members are committed to doing everything in our power to relieve DC’s heavy burden of cancer incidence and mortality. Behind the statistics is great human suffering, and that suffering must be alleviated.

Almost every part of cancer care as it relates to the medically underserved majority of residents in the District of Columbia is broken and a clear path for change must be taken if lives are to be saved.

Goals and Objectives       <top>

OVERARCHING GOAL AND PRIORITIES OF
THE DC CANCER COALITION

OVERALL GOAL: Reduce cancer incidence and mortality, reduce racial and ethnic disparities in cancer treatment, and improve the quality of life of cancer survivors by

Improving access to care

Merge the DC Health Care Alliance and Medicaid

Secure sufficient funding for the combined Alliance and Medicaid programs

Ensure every resident has a “medical home” for primary care

Provide patient navigation for cancer screening and treatment

Coordinate cancer services by linking clinics and hospitals

Improve cancer-related transportation services

Improve cancer patients’ access to clinical trials

Increasing rates of screening, particularly for breast, cervical, prostate and colorectal cancers, and providing all necessary follow-up cancer care

Increasing public awareness of healthy behaviors that prevent cancer

Reduce tobacco use

Reduce obesity

Increase regular physical activity

Eat healthy food and avoid overeating

Advocating with the City government on issues and funding relating to cancer

Educating health care providers about

Early detection of cancers

Pediatric cancers

Rehabilitation

Palliative and end-of-life care

Improving the collection and use of DC data about cancer

Improve quantity and quality of data collected about the Hispanic population

Educating survivors and caregivers about resources and follow-up care

Increasing awareness of and availability of palliative care and end-of-life care


CHAPTER GOALS AND OBJECTIVES

ACCESS TO CARE       <top>

GOAL: To improve access to primary and cancer care for DC residents.

Objectives:

1) Create a coordinated patient navigation system by 2008.

2) Establish affiliation agreements between the community health centers, hospitals, and health
 care providers for diagnostic follow-up and treatment by 2007.

3) Improve access to public transportation for cancer patients by 2010.

4) Increase the participation of eligible minority residents in cancer-related clinical trials by 15%
 by 2010.

5) Educate consumers about access to cancer screening, care, and other services by 2010.

 

PREVENTION       <top>

GOAL: Reverse the trend toward obesity and overweight by increasing physical activity and the consumption of fruits and vegetables and by reducing
caloric intake among DC residents.

Objectives:

1) Reduce the prevalence rate of obesity among DC adults to 15% by 2010.

2) Reduce the prevalence of overweight adults to 40% by 2010.

3) Reduce the prevalence rate of overweight and obese children to 5% by 2010.

4) Increase to 60% the prevalence rate of adults who engage in regular, moderate physical  activity for at least 30 minutes a day at least five days a week by 2010.

5) Increase to 40% the prevalence rate of high school students who engage in moderate  physical activity 30 minutes or more, five or more days a week by 2010.

 

SMOKING-RELATED CANCERS      <top>

GOAL: Reduce mortality from smoking-related cancers in the District of Columbia .

Objectives:

1) Reduce the level of smoking among high school students from 13% to 10% by the year 2010.   

2) Reduce the level of smoking in current Black and Hispanic smokers and those with low levels  of education by 25% by the year 2010.

3) Reduce general exposure to secondhand smoke by creating a smoke-free environment in all  public places by 2006.

4) Reduce racial disparities in smoking prevalence by 2010.


HEAD AND NECK CANCERS       <top>

GOAL 1: Reduce the mortality rate in DC from cancers of the head and neck by 10%.

GOAL 2: Reduce the incidence of invasive cancers of the head and neck in DC by 10%.

Objective:

Increase to 50% the proportion of head and neck cancers detected at the local stage for both men and women by 2010.

 

BREAST CANCER       <top>

GOAL: Reduce mortality rates from breast cancer in the District by 10%, especially among Black women.

Objectives:

1) Reduce the incidence of invasive disease in DC by 10% by 2010.

2) Increase the number of women aged 50 through 64 who are screened annually by 10%
 by 2010.

3) Reduce the proportion of unstaged cases to less than 5% by 2010.

 

GYNECOLOGIC CANCERS       <top>

GOAL 1: Identify a greater proportion of cervical cancer cases before the cancer has spread beyond the local stage.

Objectives:

1) Increase the proportion of women diagnosed at the local stage to 90% by 2010.

2) Increase the rate of Pap screening to 90% (recent screens) and 97% (ever-screened) in all
 subgroups by 2010.

GOAL 2: Make 50% of women aware that postmenstrual bleeding is a possible
symptom of endometrial cancer by 2010.

GOAL 3: Increase public awareness of ovarian cancer symptoms.

Objectives:

1) Reduce the incidence of late-stage diagnosis by 2010.

2) Improve the amount of accurate staging of ovarian cancer and reduce the proportion of
 cases classified as “stage unknown” to less than 5% by 2010.

GOAL 4: Improve the quality of care for underinsured and uninsured women in the
District who have gynecologic cancer.

Objective:

1) Increase information and support to DC clinics and providers treating the target population  by 2010.


COLORECTAL CANCER       <top>

GOAL 1: Reduce the mortality rate in DC from colorectal cancer by 10%.

GOAL 2: Reduce the incidence of invasive disease in DC by 10%.

Objectives:

1) Increase to 50% the proportion of colorectal cancer detected at the local stage for both men  and women by 2010.

2) Increase to 50% the proportion of the adult population that reports having had a fecal occult
 blood test in the previous 2 years by 2010.3) Increase to 60% the percentage of the population age 50 or older screened by  sigmoidoscopy or colonoscopy by 2010.

 

PROSTATE CANCER       <top>

GOAL: To reduce the mortality rate from prostate cancer in DC by 10%.

Objectives:

1) By the year 2010, increase to 65% the percentage of Black men 45 years or older who are  annually screened for prostate cancer.

2) By the year 2010, reduce the proportion of unstaged prostate cancer cases to less than 5%.

 

PEDIATRIC CANCERS       <top>

GOAL: To ensure that all District of Columbia children and adolescents with cancer, and their families, have access to the most beneficial medical care and supportive services.

Objectives:

1) Develop a system for coordinating research and the dissemination of information about diagnosis, clinical trials, treatment, follow-up care and supportive services to health care providers in DC by 2010.

2) Ensure that all DC childhood cancer patients and their families have access to culturally relevant information and services, from diagnosis through survivorship or end-of-life and bereavement services by 2010.

 3) Establish a system to ensure that accurate data on incidence, survival, and mortality rates for pediatric cancers are collected and are available for health care providers, researchers, and the public by 2010.


PALLIATIVE CARE       <top>

GOAL 1: Integrate palliative care into the District’s health care system and increase public understanding of palliative care and its role in cancer care.

Objectives:

1) Provide education about palliative care for health care providers and the public by 2010.

2) Promote the development of palliative care programs in health care facilities and community- based settings throughout the District by 2010.

3) Develop innovations and changes in the health care delivery system that promote palliative  care services by 2010.

GOAL 2: Improve the availability of, and access to, palliative care services for the underserved and culturally diverse population of the District of Columbia by 2010.

Objectives:

1) Strengthen the health care delivery system, including palliative care for underserved and  diverse populations in the District of Columbia by 2010.

2) Target public service messages about palliative care to specific underserved populations  by 2010. 

CANCER SURVIVORSHIP      <top>

GOAL: Improve the quality of life for DC cancer survivors.

Objectives:

1) Implement a coordinated patient navigation system by 2008.

2) Increase demand-responsive public transportation for low-income cancer survivors by 2007.

3) Assess current resources for survivors and caregivers by 2006.

4) Promulgate clinical practice guidelines for each stage of cancer survivorship, from diagnosis through long-term treatment and end-of-life care by 2007.

5) Establish a database on cancer survivorship by 2008.

6) Educate corporate, academic, and community policymakers and decision-makers about key  health care issues for cancer survivors by 2008.

7) Develop a community awareness program for cancer survivors by 2007. 

CANCER REHABILITATION       <top>

GOAL: Increase awareness of cancer rehabilitation services in the District of Columbia .

Objectives:

1) Create a repository of information on cancer rehabilitation services in the District of Columbia by 2007.

2) Increase awareness and knowledge of fellows in training, oncology physicians, and oncology nurses about cancer rehabilitation and services by 2008.

3) Increase public awareness of cancer rehabilitation and services available by 2009.

4) Develop liaisons among area hospitals and community organizations to conduct research on  effective cancer rehabilitation assessment and treatment by 2010.

 

Introduction:


Text Box: Developing a Cancer Control Plan
for the District of Columbia


To address the problem of very high rates of cancer in the District of Columbia , in 2001 the DC Department of Health (DOH) created the DC Cancer Coalition. The Coalition was born when the DOH and other stakeholders attended a leadership institute sponsored by the Centers for Disease Control and Prevention, the American Cancer Society, the National Cancer Institute, and the American College of Surgeons. There we learned more about how to develop and implement comprehensive cancer control programs that integrated partnerships, communication, and collaboration. In 2003 the Department of Health received an initial grant for cancer planning from the CDC—and the Coalition began its work.

Committed to addressing the District’s very high cancer rates—the highest cancer death rates in the nation—the Coalition is a broad-based partnership, including medical centers, nonprofit organizations, academic and research institutions, community groups, advocates, professional organizations, and others. All have an interest in cancer prevention and control. Our objective has been to develop a comprehensive cancer control plan that could serve as a blueprint for reducing the number of new cancer cases in the District and the number of deaths from cancer. We have followed the CDC’s model of creating “an integrated coordinated approach to reducing cancer incidence, morbidity, and mortality through prevention (primary prevention), early detection (secondary prevention), treatment, rehabilitation, and palliative care.” The Plan is designed to

Identify the strengths and weaknesses of current cancer prevention and control efforts in DC

Identify barriers that hinder prevention and control efforts and offer strategic options for surmounting them

Provide a set of goals and objectives for cancer control based on a review of DC data

Identify strategies for meeting those objectives.

Disparities in cancer care in DC:
Demographics and access

The District is home to an abundance of medical care facilities and providers, but equal access to cancer care services is significantly undermined by the physical location of those providers. Access to cancer screening, treatment, and follow-up care is, in some measure, influenced by where a District resident lives.

Geographically, the District is divided into four quadrants: northwest, northeast, southwest, and southeast. Politically, it is divided into eight wards (see Figure 1). Wards 1, 3, and 4 are in the northwest quadrant; Ward 2 straddles northwest and southwest; Ward 5 is mainly in the northeast (and a bit of northwest): Ward 6 is in northeast, southwest, and southeast; Ward 7 is in both northeast and southeast; and Ward 8 is in the southwest and southeast quadrants.

Many cancer-related health care facilities are located in northwest Washington (in Wards 1, 2, 3, 4, and parts of Ward 5). There is just one



 

  dc
 


full-service hospital located beyond the Anacostia River (Wards 7 and 8), serving 20% of the District’s population. For those dependent on public transportation, especially those weakened by cancer, it can be difficult and exhausting to reach a hospital in another part of the city. One District hospital, Providence , is in the northeast quadrant. Another, Greater Southeast Community Hospital, is in southeast. The other nine—Children’s National Medical Center , George Washington University Hospital , Georgetown University Medical Center , Howard University Hospital , National Rehabilitation Hospital , Sibley Memorial Hospital , Veterans’ Affairs Medical Center , Walter Reed Army Medical Center , and the Washington Hospital Center —are all in the northwest. All four cancer centers— Georgetown , George Washington, Howard and Washington Hospital Center —are located in the northwest.

The inequitable distribution of infrastructure for cancer care in the District is reflected in the city’s cancer incidence and mortality rates. Disparities in access to care and in the quality of care are seen in every aspect of cancer control: screening, early detection, incidence, treatment, quality of care, and survival. Disparity issues are considered in nearly every chapter of the Cancer Plan. We expect implementation of the Plan to facilitate the creation of an effective local infrastructure for reducing these disparities, for reducing high cancer incidence and mortality rates in the District, and for improving the quality of life of cancer survivors—wherever in the city they may live.

Ethnicity. As of 2004, DC’s population
was 58% Black, 27% White, and 3% Asian. Another 2% describes themselves as “two races or other.” About 10% of the population is Hispanic (some self-identifying as White, some as Black). The Hispanic population, which is the fastest growing segment in the city, is located mainly in Wards 1 and 4.

Income. Although the city’s population is distributed roughly equally among the eight wards, income distribution is unequal. A
significant number (roughly 147,000 or 26%) of residents have household incomes below
$20,000 a year. The high cost of living in Washington places households earning less than $20,000, especially those with earnings below $10,000, in extreme poverty. Average
per capita income is highest in Ward 3 ($68,477) and lowest in Ward 8 ($14,137). Similarly, average household income is
highest in Ward 3 ($134,506) and lowest in Ward 8 ($38,754).

Education. Almost 300,000 Washingtonians—
22% of those older than 25—do not have a high school diploma. The highest number of people with college degrees is reported in Ward 3 (79%), and the lowest in Ward 8 (8%).

 

Developing the Cancer Plan

To develop the Plan, the Coalition created
multidisciplinary workgroups (physicians, public health experts, community leaders, survivors, representatives of advocacy groups, nurses, social workers). Each workgroup developed a chapter of the Plan, reporting its findings to the full Coalition. The Coalition developed a list of objectives for cancer control based on a review of research data and identified strategies for achieving those objectives. We carefully evaluated the cancer burden in the District, analyzed tumor registry data on incidence and mortality, reviewed national data on cancer, catalogued existing resources for screening and early detection, considered the impact of disparities on health care, and sought out community leaders for advice and direction. We looked at modifiable and nonmodifiable risk factors for specific cancers, discussed control strategies based on evidence, examined approaches to health communications, categorized clinical services, compared survival rates, and built partnerships.

Primary focal points. The Plan’s primary focus was on strategies known to reduce the number of cases of cancer and to reduce deaths from the disease. Recommendations for cancer screening were based mainly on those of the American Cancer Society, although recommendations from the Preventive Services Task Force and other professional organizations were also reviewed. A secondary focus was to identify resources to assist people with cancer, including support groups, educational programming, and other community opportunities. These resources are presented in a separate publication, the
Community Resource Directory for Cancer Survivors and Caregivers.

Based on data about the burden of cancer and available health care resources in the  
District, we established cancer site priorities for DC’s Cancer Plan of breast, cervical, colorectal, smoking-related cancers, head and neck cancers, and prostate cancer.

Priorities were based on scores of four factors:

The extent of a particular cancer burden

Whether intervention was important

Whether intervention was feasible

Whether intervention would have a measurable impact (that is, reduce incidence and/or mortality rates).

The burden of deaths from smoking-related cancers, for example, is sizable. Effective intervention is feasible, and its impact would be large and measurable. Similarly, the burden of prostate cancer is the District is both heavy and inequitable, and effective intervention is solidly feasible and measurable. Breast cancer interventions are a priority because the cancer burden is heavy, mammography is
a fairly effective screening tool, screening reduces mortality, and effectiveness is measurable. Interventions to deal with colorectal cancer, a major problem in the District, are more difficult. The best way to intervene is through a citywide colonoscopy program. This would be very expensive and
is therefore more difficult to implement— although efforts to educate physicians and patients about the value and importance of screening can have a positive effect.

For each type (or anatomical site) of cancer, we looked at risk factors, gaps in and barriers to cancer control, and the best-known
prevention and control measures, before we identified goals, objectives, and strategies for that type of cancer. We also addressed access to care, what to do about smoking-related cancers, how to support and improve the quality of life for cancer survivors, how to improve palliative and end-of-life care, and how to integrate cancer rehabilitation services into overall cancer care.

The chapters were reviewed for accuracy
and completeness by physicians and other health care professionals not associated with the Coalition, as well as by lay consumers.
The Coalition is deeply indebted to these reviewers for time-consuming efforts that, they surely know, will benefit many. As part of its mission, the Coalition will review the Plan regularly and modify priorities to reflect new data, new scientific knowledge, and the availability of more or different resources. We have included an evaluation component, so we can measure progress.

In the summer 2005, the DC Cancer Coalition held a series of five town hall meetings in neighborhoods around DC to introduce the Plan, to listen to residents’ thoughts and reactions to the Plan and to encourage residents to get involved in fighting cancer in the District. The Department of Health also held a series of Health Disparities Town Halls at which they announced the Plan and invited residents to become involved in implementing the Plan.

The Coalition is pleased to present this Plan to the citizens, community leaders, and city authorities of the District of Columbia . We
look forward to constructive comments and approval of the Plan’s objectives and
strategies, and to creating innovative,
speedy, and effective actions for the next phase of our work—implementing the Plan. The District now joins 27 states that have
developed cancer control plans.

 


Text Box: Access to Care       <top>


Great therapeutic developments over the past few decades have led to more effective and less disfiguring cancer treatments. But not every American has benefited from this
progress, as evidenced by higher cancer incidence rates and lower survival rates in certain populations. Poor people lack access to health care and are more likely than others to die of cancer, reported the American Cancer Society in its 1989 report, Cancer in the Poor.
Moreover, poor people are less likely to be covered by health insurance and often do not seek care if they are unable to pay for it.

In 2004, the number of insured nationally rose to 45.8 million, compared to 45.0 million in 2003 and 39.8 million in 2000. A continuing decline in employer-sponsored plans is a major cause. The percent of working adults (18 to 64) who were uninsured climbed from 18.6% in 2003 to 19.0 percent in 2004, an increase of more than 750,000 people. Nationwide, African Americans (20%) and Hispanics (33%) were much more likely to be uninsured than White, non-Hispanic people (11%).

Reducing cancer incidence and mortality rates in the District of Columbia will require eliminating barriers to primary and cancer
care for all DC residents, but especially the medically underserved—the poor, the uninsured, and the culturally isolated. Only with accessible, affordable personal health care services can DC residents hope for the best possible health outcomes.

Barriers to care in the District

Demographics—insurance coverage, poverty, education, race, language, age, and gender— explain many DC residents’ failure to get adequate health care. Lack of knowledge and information about sound health practices may also keep many residents from getting the care they need.

Lack of health insurance. Whether DC
residents have access to good health care often depends largely on whether they have health insurance coverage. Lack of insurance
or underinsurance (lack of full coverage or limited access to health care) is the most significant factor contributing to disparities in cancer care.

In 2004, the number of insured nationally rose to 45.8 million, compared to 45.0 million in 2003 and 39.8 million in 2000. A continuing decline in employer-sponsored plans is a
major cause. The percent of working adults (18 to 64) who were uninsured climbed from 18.6% in 2003 to 19.0% in 2004, an increase of more than 750,000 people. Nationwide, African Americans (20%) and Hispanics (33%) were much more likely to be uninsured than White, non-Hispanic people (11%).

Proportionately, more DC citizens are covered by employer-sponsored insurance than the national average because of the concentration of federal agencies and offices in the District. Of DC’s non-elderly adults, 70% have employer-
sponsored or self-paid insurance, 11% have Medicaid, 13% have no insurance and 5% fall into an “other” category. The number of uninsured non-elderly adults in DC (74,200) can swell by thousands throughout the year, as some residents temporarily lose their health insurance during a hiatus in employment. 

Of those with no health insurance, 4% are enrolled in the DC HealthCare Alliance, a public-private partnership established after DC

General Hospital closed, to improve access to care for the uninsured. The Alliance suffers from insufficient funding and an inability to contract with specialists, such as oncologists, because of very low rates of reimbursement and very long delays in providing reimbursement.

Who are the uninsured?

In 1999, 60% of DC adults may have qualified for Medicaid or DC HealthCare
Alliance coverage, based on income. (Adults with children are eligible for Medicaid if their income falls below 200% of the federal
poverty level.) DC Medicaid also provides some coverage for low-income, non-parent adults.

In 1999, 36% of DC adults over age 65 had income that fell below 200% of the federal poverty level, possibly qualifying them for Medicaid.

The number of Medicaid enrollees in DC represented 81% of the eligible population in 2001, according to the Centers for Medicare and Medicaid Services.

Many of the “working poor” are uninsured: 72% of uninsured DC residents are part of family households in which at least one household member works part- or full-time, and 48% of the uninsured have family members who work full-time, year-round.

The largest group of uninsured adults (29,500) is 30-to-49-year-olds, but another age group, the 19-to-29-year-olds, has the greatest percentage of uninsured. The two groups with the most uninsured members are Hispanic residents (about 13,800
residents, or 33.4% of the local Hispanic population) and non-Hispanic Blacks (with 50,200 residents, or 16.7% of non-Hispanic Blacks), as Table 1 shows.  

Undocumented aliens have no health insurance. Although they can receive free or low-cost health care at a community health center, the center will ask them to apply for Medicaid so it can recover some of its costs. Undocumented residents are reluctant to apply for a public program because it
might mean having to divulge reportable information. If an undocumented alien visits the emergency room, he will be served. If he has to be admitted to the hospital, the admitting physician will have to follow the patient at no charge.

In the year 2000, 13% of DC residents worked for small-business employers, who were less likely to offer insurance because
of the high cost of premiums. About 63% of DC residents worked in service and retail positions that did not offer health insurance benefits.

Some low-wage earners have to forfeit health insurance benefits because they cannot afford the employee’s share of the premium.

About one-third of DC’s non-elderly adults went without health insurance for all or part of the two-year period from 2002 to 2003. Adults with no insurance and those with Medicaid are more likely than adults with
private health insurance to report that they are in poor to fair health (18%, 29%, and 7%, respectively).

Residents with some health insurance may not have coverage for pharmaceuticals, durable medical equipment, nutritional supplements, sub-acute care, long-term care, or mental health services. Medicare
is the largest health insurance program with only partial coverage.

Some adults don’t seek treatment or care because they can’t afford the cost of co-payments or out-of-pocket expenses for items that are not covered.


Poverty, race, and socioeconomic status. Race and ethnicity themselves are not
barriers to primary and cancer care, but minority status associated with poverty or
with negative perceptions of the health care system may affect outcomes. As Mandelblatt and colleagues observe, some Hispanic and Black populations are either fatalistic about cancer or are too preoccupied with day-to-day survival to seek early detection or treatment.

Levels of education and literacy, especially health literacy, are important aspects of social status that affect health outcomes. The
Annals of Internal Medicine reported that literacy skills predict an individual’s health status more strongly than age, income, employment status, race, or ethnicity. Poor literacy impedes people’s ability to learn about disease prevention, understand disease- related information, follow physicians’ instructions, take medications properly, and self-manage health care.

Socioeconomic status is also a factor.
Regardless of other factors, people in lower socioeconomic groups report less use of
cancer screenings and are diagnosed with cancer at later stages than those in higher socioeconomic groups—even in Canada and Finland, countries with universal health care coverage.

Socioeconomic status also appears to affect the quality of care. People from lower socioeconomic groups also have poorer survival rates, possibly because of such factors as inadequate staging evaluation and delays in treatment. Regardless of treatment, cancer patients from lower socioeconomic groups with advanced cancer report less symptom control and less use of palliative and supportive care services (especially hospice) than patients from higher socioeconomic groups.

The percentage of uninsured in DC (13%) is lower than the national average (19%), but the
 percentage of residents who live in poverty (20.3%) is higher than the national average

 


(12.4%). Although the city’s population is distributed roughly equally among eight wards, income and relative insurance status are
distributed unequally (see Table 2).

Unfortunately, the poverty gap—the gap between the wealthy and poor—is as wide in DC as in any other major U.S. city, and the gap is widening. The average income of DC’s wealthy families grew 38% in the 1990s; the income of poor families grew only 3%.

The adult populations in DC most likely to be uninsured are poor, male, and Hispanic or Black. The Hispanic population is particularly vulnerable, having the highest uninsured rate, being poorer than non-Hispanic Blacks or Whites, and having worse health indicators than both groups.

 

Language. Residents of the District of Columbia , many of whom are recent immigrants or temporary residents, come from more than 150 countries. This enriches the culture but creates linguistic challenges. A health care center, despite federal requirements to provide qualified interpreters, often cannot provide interpreters for every language. Even if an interpreter is available, the interpreter may know a word but not in a medical context, and the health care provider may not appreciate the cultural nuances of each phrase or topic. What’s more, people from some countries may consider the direct and candid U.S. style of communication too forward or impolite. There is, therefore, sometimes a reduced chance of clear
communication.


 


Age. Although 77% of all cancers are
diagnosed in people 55 and older, older people may not realize their risk of cancer,
may ignore symptoms, and may suffer from cognitive impairment and other medical
conditions. And proportionately more of the elderly are poor and underinsured. Any of these factors may limit older people’s pursuit of early detection or cancer treatment. And as the senior population grows, age will become a more significant barrier to good primary and cancer care. Heavy concentrations of adults 55 and older live in Wards 3, 4, 5, and 7
(see Table 3).

Gender. Evidence shows that men seek routine preventive medical care less often than women, but research has shown practitioner bias in screening men for cancer more often than women.

Culture. People immigrating to the District from other countries bring with them a host of customs, attitudes, and health care practices that can affect their health care here. Poor immigrants, especially when confronted with a complex health care system managed in a language different from their own, may simply avoid or minimize contact with it except in emergencies, and rely on practices they know from their own cultures. Similarly, the pressure of urgent daily priorities such as food, employment, transportation, education, housing, and safety may mean that cancer screening for early detection becomes a
relatively low priority.     

Transportation. Barriers to screening or cancer care can be as basic as not
having transportation to an appointment with a physician or to purchase essential medications. Many patients do not have their own private means of transportation and their family members may work or may also not have a means of transportation. Public transportation is widely available in the District, but it often requires a far greater commitment of time—time away from work and from family—than arriving by private automobile would, for example. When the requirements of time are combined with the exhausting side effects of cancer treatment, transportation becomes
a significant barrier. Moreover, demand- responsive transportation for cancer patients and disabled persons is limited in the District, and some volunteer drivers of agency transportation programs and taxicabs will not travel into neighborhoods they perceive
as dangerous.

Barriers to care from primary care and cancer care providers

Problems among primary care providers and oncologists may limit some patients’ access to good health care.

Physician competence, knowledge,
attitudes, and beliefs.
The greatest predictor of patient compliance with cancer screening
is a physician’s recommending a cancer screening test. But whether a primary care provider recommends such a test may be
affected by:

The provider’s biases and beliefs about screening and treatment effectiveness

Insufficient knowledge, training, or skill (performing a clinical breast exam, for example)

A dearth of culturally sensitive resources

Forgetfulness and lack of time

Concern about the patient’s other acute
illnesses

Conflicting screening guidelines from
professional and health organizations

Concerns about patient acceptance

No chance of reimbursement

Logistical or organizational barriers

Prejudices based on age, race, gender,
or sexual orientation

Inadequate communication skills.




Too few health care professionals and services in low-income neighborhoods. As of 2001, DC had the highest physician-to-population ratio of any state, but most of those physicians do not work in low-income neighborhoods (see Table 4 for location of clinics by ward). According to the Bureau of Primary Care of the U.S. Department of Health and Human Services, 300,825 DC residents (52% of the total population) live in federally designated primary care Health Professional Shortage Areas (HPSAs) and 173,228 (30%) live in federally designated Medically Underserved Areas (MUAs). Areas designated HPSA and MUA tend to include many poor households and homes of racial and ethnic minorities.

A lack of “medical homes.” Many of the 300,000 District residents identified as living
in a Health Professional Shortage Area do
not have a “medical home”— a primary care provider who knows a patient’s health history and is a reliable source of non-emergency medical care. The DC Primary Care
Association (DCPCA) has linked the lack of adequate primary care in DC to poorer health outcomes, higher health care costs, and overused and crowded emergency rooms. “Because people can’t find a doctor,” explains the DCPCA, “they delay care, escalating the severity of the illness to crisis and contributing to high disability rates.”

Too few specialists serving poor neighborhoods. The DC HealthCare Alliance has difficulty enrolling and maintaining oncologists and other specialists, who feel the insurer’s reimbursement rates are too low and slow.

Problems intrinsic to the local health
care system

When DC General Hospital closed in 2000, its patients were transferred to DC’s remaining hospitals. All the hospitals in DC accept Medicaid and DC HealthCare Alliance patients. When hospitals serve these
populations, they are required to serve them in the emergency room as well. Seven percent (7%) of DC residents identify the emergency room as their primary source of medical care. A greater proportion of uninsured DC residents
use the emergency room as their regular source of medical care than do insured residents.



DC prides itself on its many private and public community health centers that provide excellent primary care. The weakness of the community health centers is that they are only loosely linked to each other and to other parts of the health care system for services such as diagnostic follow-up, cancer treatment, behavioral health, transportation, counseling, pharmacy or hospital services. As a default, patients may use hospital emergency services that are more expensive and more traumatizing to the patients.

Text Box: Even an educated person, astute about health care, can havetrouble navigating the labyrinth of health care resources, regulations, and procedures in the U.S. health care system, as well as complying with instructions from multiple physicians. Timing and follow-up are also issues in health care centers, where it often takes too much time to arrange for diagnostic follow-up, treatment, and post treatment care. For lack of equipment and expertise to handle billing adequately, community health centers have at times had difficulty submitting timely program and financial information to contractors and health plans. Project WISH, the DC Breast and Cervical Cancer Early Detection Program, lost funding temporarily because it did not receive timely reports from community health centers that are Project WISH provider sites.

On the other hand, community health centers often have difficulty retrieving reports from
specialists, especially those in hospitals, on
Alliance and Medicaid patients they serve. There is controversy about who owns the
information, suspicion about how the information will be used, and little cooperation among some health care providers. There is a strong sense in general that the community health centers want to strengthen their links to hospitals, the DC HealthCare Alliance, specialty providers, and the DC Department of Health.

Even an educated person, astute about health care, can have trouble navigating the labyrinth of health care resources, regulations, and
procedures in the U.S. health care system, as well as complying with instructions from multiple physicians. Sometimes a family member or friend has the time and ability to help a
patient maneuver through the health care
labyrinth and even to serve as the patient’s advocate. But add a complex medical condition and/or language, cultural, and financial barriers and the patient, overwhelmed, may drop out of part or all of the health care system.

Professional or lay “patient navigators” can help a patient through the system if a competent family member or friend cannot. Especially with medically underserved and vulnerable populations, patient navigation has been effective in improving access to good care. A few community health centers and DC’s Project WISH successfully use patient navigators. But the need for patient navigation far outweighs current resources.

Reimbursement and funding problems. After DC General Hospital closed, a program called the DC HealthCare Alliance was created to offer health care to uninsured DC residents whose income is 200% of the federal poverty
level or less and who are not eligible for Medicaid or Medicare. In the DC HealthCare Alliance, through a partnership with the DC Department of Health, private and nonprofit community health centers offer access to inpatient hospital care, outpatient medical care (including preventive services), emergency services, prescription drugs, rehabilitative services, home health care, dental services, specialty care, and wellness programs
(including pre- and post-natal care).



But the Alliance faces certain challenges:

Because the city chronically underfunds the Alliance , it has never been able to enroll all eligible persons.

It added no additional community health centers or physicians to DC’s medical
infrastructure to serve the eligible population.

It has had difficulty enrolling specialists in its network of physicians because of low and slow reimbursements.

It does not reimburse physicians who serve DC HealthCare Alliance or Medicaid patients in the emergency room.

It reimburses hospitals and physicians slowly and at far below the actual cost of care (15 cents on the dollar), so hospitals have to absorb millions of dollars in uncompensated care each year. Providers have little incentive
to provide additional services to patient groups that do not generate revenue.

Another support service for District residents is the Archdiocesan Health Care Network, whose mission is to connect uninsured patients seen in their clinics with appropriate specialists and tests. This network has several hundred physician-specialist volunteers who will see patients from the clinics for workups and in some instances will provide surgery and follow-up care.

Regional resources and clinical trials. DC is fortunate in having eleven hospitals that
provide cancer care. Lombardi Cancer
Center (at Georgetown ) has been designated a comprehensive cancer center by the
National Cancer Institute. Other cancer
centers include George Washington University Cancer Center , Howard University Hospital Cancer Center , and the Washington Hospital Center Cancer Institute. Three hospitals have medical schools and four are teaching

hospitals. The cancer programs of eight hospitals are approved by the Commission on Cancer of the American College of
Surgeons. Because of the quality and quantity of hospitals in DC, numerous cancer-related clinical trials offer state-of-the art cancer care, potentially improving access to quality care for the medically underserved and reducing disparities in cancer care among racial and ethnic groups. Historically, however, minorities and females are severely underrepresented
in clinical trials, for various reasons. The literature has identified the barriers to minority participation in clinical trials and strategies
for overcoming these barriers. There is no legislative mandate for insurers in DC to cover the routine costs of patient participation in clinical trials.

Community health centers. Half of the community health centers in DC offer early morning hours, 38% offer evening hours, and one-third offer Saturday hours. Ward 1 has the most community health centers; Ward 4 has none. In the District, there are

Three federally qualified health centers (FQHCs) with 28 sites

Three hospital-sponsored health centers with 14 sites

Eleven private, nonprofit centers with 12 sites

Twelve uncategorized clinics.

In the fall of 2003 the DC Primary Care
Association reported that 52% of the FQHCs, 80% of the hospital community health
centers, and all of the private nonprofit
community health centers could not meet
current needs with existing resources.

 

 

 

Limited screening programs and
facilities in poor neighborhoods.
Despite the District’s  very high cancer incidence and mortality rates, the DC Department of Health underfunds screening programs for breast, cervical, and prostate cancers and provides no funding for screening for colorectal cancer. Most screening resources are located north
of the Anacostia River . Many of the poorest DC neighborhoods are southeast of the
river. In Southeast DC, there is only one
mammography facility: the Capital Breast Care Center . The remote location of most screening sites is a barrier to increasing cancer screening rates, especially for women who have difficulty
taking time off from work or arranging for transportation and child care.

Problems filling prescriptions. Two
organizations in DC (Rx4DC.org and DC
Pharmaceutical Resource Center) help
uninsured residents identify and apply to
pharmaceutical companies that provide free medications to residents who are low income,
are uninsured, or receive Medicaid. One
problem is that pharmacies in some low-
income neighborhoods do not stock
prescription pain medications for fear of
burglary related to substance abuse. This means that cancer patients who need
these medications face additional hurdles obtaining relief.

Progress

The Department of Health reports that a
number of steps have been taken to further integrate and improve the Alliance and
Medicaid, including appointment of a single Medical Director, adoption of HEDIS measure reporting, implementation of new waivers, use of managed care organizations, and dual use of Income Management Administration. The DOH further notes that the Department is in the midst of a major reform of the DC Alliance that will take effect in 2006.

Meanwhile, the DC Primary Care Association, with significant support from the DC
Department of Health, has launched a
Medical Homes Initiative to strengthen the infrastructure of the community health
centers network. The citizens who
developed the DC Cancer Plan wholly
support these efforts, including the DC
Primary Care Association’s plans to establish a coordinated, citywide database to track patient information.

 

 

 



Goals, Objectives, and Strategies

GOAL: To improve access to primary and cancer care for DC residents.

Objectives and strategies:

1) Create a coordinated patient navigation system by 2008.

Seek funding for coordinated patient navigation in hospitals and community health centers.

Develop a coordinated patient navigation system.

2) Establish affiliation agreements between the community health centers, hospitals,
 and health care providers for diagnostic follow-up and treatment by 2007.

Facilitate negotiation of these affiliation agreements.

3) Improve access to public transportation for cancer patients by 2010.

Work with the Washington Metropolitan Area Transit Authority (WMATA) to expand its
demand-responsive system.

4) Increase the participation of eligible minority residents in cancer-related clinical
 trials by 15% by 2010.

Advocate for legislation requiring insurers to cover routine patient costs for clinical trials.

Update health care providers on clinical trials and encourage patient referrals.

Launch an awareness and recruitment campaign focused on racial and ethnic populations, particularly Blacks and Hispanics.

5) Educate consumers about access to cancer screening, care, and other services
 by 2010.

 

References

Adams-Campbell LL et al. Enrollment of African Americans Onto Clinical Treatment Trials: Study Design Barriers. Journal of Clinical Oncology. 2004;22: 730-734.

American Hospital Association. District of Columbia : Hospital Emergency Room Visits per 1,000 Population by Ownership, 2002. Available at: <www.ahaonlinestore.com/ProductDisplay.asp?ProductID=637&cartID=173831>. Accessed October 7, 2004.

Cohn, D’Vera. “DC Gap in Wealth Growing,” in Washington Post, July 22, 2004 <www.washingtonpost.com/wp-dyn/articles/A4052-2004Jul21.html>.

DC Office of Planning. 2000 Population by Age by Ward. Available at:< <www.planning.dc.gov/planning/cwp>. Accessed January 7, 2005.

DC Primary Care Association. Primary Care Safety Net: Health Care Services for the Medically Vulnerable in the District of
Columbia
. October 2003.

Families USA. Who’s Uninsured in the District of Columbia and Why? Available at:
<www.familiesusa.org/site/DocServer/DC_uninsured.pdf?docID=2368>. Accessed September 6, 2004.

Kaiser Family Foundation, The Henry J. Coverage and Access of Adults 18-64 in the District of Columbia : Key Facts, #7083.
Available at: <www.kff.org/minorityhealth/loader.cfm?url=/commonspot/security/getfile.cfm&PageId36035>. Accessed
October 11, 2004

Lurie N, Stoto M. Health Insurance Status in the District of Columbia . Report conducted by RAND under contract from District of Columbia Primary Care Association, 2002.

Mandelblatt JS, Yabroff KR, Kerner JF. Equitable Access to Cancer Services. Cancer 1999;86:2378-2390.

Rivera P, Billington M. Curanderas Offer Traditional Help. Wilmington , Delaware News Journal; January 27, 2003.

Wilson JF. The Crucial Link Between Literacy and Health. Annuals of Internal Medicine 2003; 139(10): 875.


Cancer Prevention

Facts in brief

Text Box: There is a growing body of epidemiological evidence suggesting that factors
contributing to the development of cancer (as well as undermining overall health) include:

Smoking and overconsumption of alcohol (especially combined)

Overexposure to ultraviolet light (through sunlight or tanning salons)

Overconsumption of red meat, especially when charred

Overconsumption of fat and sugar

Consumption of food cooked with harmful fats.

Insufficient consumption of fruits, vegetables, and whole grains—rich in vitamins, antioxidants, and minerals that may help slow or prevent the development of cancers.

Too little physical activity.

dc
 

 



Cancer has now surpassed heart disease as the nation’s number one killer for persons age 85 or younger. Coronary heart disease
declined significantly after 1973, largely through changes in people’s behavior—
and it is not unreasonable to think that a
similar decline in cancer incidence could occur if individuals changed to behaviors that appear to help prevent the disease: sound nutrition, no smoking, maintaining reasonable weight, minimal or no alcohol consumption, adequate, regular physical activity, and limited exposure to the sun. By some estimates, poor nutrition, physical inactivity, and obesity together
account for roughly a third of all cancer deaths, and the use of tobacco another third.
Prevention eliminates many problems and costs down the line, but it must be started early. The best way to prevent lung cancer, for example, is never to smoke. An ounce of prevention truly is worth a pound of cure—
reducing illness, prolonging a healthy life, and maintaining a satisfactory quality of life.

 

 

American health has declined as Americans have shifted increasingly to a diet of foods high in fat, sugar, and refined grains—the staples
of fast food restaurants that serve oversize portions to vast numbers of Americans. Almost a third of all children and teenagers consume fast food on a typical day.

Current dietary recommendations include minimal fats and red meat and plenty of fruits, vegetables, and whole grains. Fruits and
vegetables are probably protective because
of their fiber content, micronutrients, and
colorful phytochemical compounds, such as the lycopene in tomatoes, the folates in leafy green vegetables, and the flavonoids in citrus. Not all valuable dietary factors have been
isolated, so vitamin supplements may not be as valuable as whole foods.

The type of fat consumed matters to general health, as well. Authorities recommend that foods be prepared with such fats as olive oil, canola oil, and safflower oil.

 

 

Text Box: In the District of 
Columbia in 2003, 52.4% of adults 
were identified 
as overweight or 
obese, up from 
50.5% in 1998. Diets high in fruits, vegetables, and whole grains reduce the risk of cancer—especially cancers of the colon, esophagus, lung, and oral cavity. According to the National Cancer Institute’s “Eat 5 to 9 a Day for Better Health” Program, to reduce risk people should consume at least five to nine servings a day of vegetables and fresh fruits, such as citrus, yellow and green leafy
vegetables, soy products, and whole grain wheat products. A serving is approximately that amount that fits in the palm
of the hand.

Surveys show that only 23% of adults and 21% of the young consume the minimum five daily servings of fruits and vegetables recommended by the National Cancer Institute. In Washington DC , only 29.5% of adults and 21.3% of the young (in 2003) consumed at least five servings of fruits and vegetables daily. Most people consume only two or three servings, and some none at all (USDA, 1998).

Overweight as a risk factor

Lifelong eating behaviors develop early in childhood. According to surveys conducted by the Centers for Disease Control, many DC teens aged 12 to 17 are at risk or already overweight. Rates are especially high among Hispanic and Black teens. Improving the
nutrition and physical activity practices of
children and adolescents is important for
promoting their long-term health.

Concern is growing about obesity’s effect on cancer, heart disease, and stroke. Obesity rates among adults increased 75% between 1991 and 2001. In the last 20 years, the rates have doubled in children and tripled in teens. The prevalence of obesity in men is the same among all racial/ethnic groups, but in women the prevalence is highest among Blacks. More than half of Black women over 40 are obese and 80% are overweight.

 

 

The American Cancer Society estimates that obesity accounts for 14% of all cancers in men and 20% of those in women in the United States .

In the District of Columbia in 2003, 52.4% of adults were identified as overweight or obese, up from 50.5% in 1998—mirroring
nationwide trends that cut across both genders, all ages, and racial and ethnic groups.

Obesity trends among
children will influence future rates among adults. Chances are that individuals who are overweight as children or young adults will be overweight as adults. In 2003, 11.5% of DC high school students were overweight and
another 17.3% were at risk of becoming overweight. Rates are especially high among Latino and Black teens.

Smoking and alcohol

In hundreds of studies, smoking has been
implicated as a cause of cancers of the lung and upper respiratory tract and is also
associated with cancers of the large intestine, bladder, and pancreas. Investigators estimate that 30% of all U.S. cancer deaths are
attributable to smoking.

Alcohol is known to interact with tobacco smoke in causing cancers in the oral cavity, upper respiratory tract, throat, and gastrointestinal tract. Alcohol and smoking have also been associated with second cancers arising in the mouth and throat after a first mouth or throat cancer has been treated. The most effective way to prevent cancers of the mouth and throat is to avoid tobacco and drink minimal amounts of alcohol. Alcohol has also been associated with cancers arising in the large intestine and pancreas, although the evidence is not as strong as with cancers arising in the head and neck.

 

 

There is also evidence that alcohol may increase the risk of breast cancer in postmenopausal women.

Physical activity

Regular physical activity is an important
factor in maintaining healthy weight and body composition. DC residents are not presently achieving recommended levels of regular physical activity. Survey data show that in 2003 half of DC adults engaged in
moderate-intensity physical activity for 30 minutes or more at least 5 days of the week. The association between physical inactivity and cancer is weak, but physical activity has been shown to help prevent obesity, which is strongly associated with cancer. Over half of DC residents are not participating in enough physical activity to reap significant benefits.

There is a clear relationship between physical
activity and risk of colon cancer: the more physical activity, the lower the risk of colon cancer.

Physical activity is also important in cancer treatment and rehabilitation, helping to
improve mood, functional ability, quality of
life and reducing fatigue, body weight, and
the severity of some side effects.

The 2001 Shape of the Nation Report issued by the National Association for Sport and Physical Education strongly recommended physical education for grades K through 6.
Although 95% of the lower grades have
physical education programs, they provide only about 40 to 50 minutes of exercise a week. Middle and high school levels require a physical education program, but the high school requirement extends only through grade 10, providing for 60 fifty-minute classes for ninth grade and 120 fifty-minute classes for tenth grade.

 

 

 

 

Physical education grades are included in the grade point average. No other activity substitutions are allowed.

Avoiding overexposure to the sun

The most common carcinogen to which people are exposed is sunlight (especially ultraviolet light). Overexposure to sun has been associated with all forms of skin cancer, the most common cancer in humans. Most skin cancers can be treated; only one, melanoma, is difficult to treat and, when advanced, carries a high death rate. Since 1973 the rate of
melanoma has been increasing in adults, young adults, and teenagers—especially among Whites. Presumably, the rising rate is the result of increased exposure to ultraviolet light either through sunbathing, overuse of
tanning salons, and partial loss of the ozone layer. Frequent sunburns during childhood may increase the risk of melanoma or other skin cancers that occur years later. The routine use of sun block, which blocks ultraviolet light, is strongly recommended. The best prevention, however, is avoiding too much sun (especially in childhood) and not frequenting tanning salons.

Chemoprevention

Agents designed to prevent cancer or to inhibit growth of precancerous lesions are under extensive investigation. The National Cancer Institute, for example, is conducting a
clinical study to determine whether selenium and vitamin E can prevent prostate cancer. Laboratory and clinical observations support the use of ordinary aspirin for the prevention
of colon cancer, breast cancer, and lung
cancer. Aspirin use must be balanced against potential complications such as internal
bleeding and allergic reactions, but daily use
of a single tablet of aspirin for life may reduce the risk of both cancer and heart attacks.

 

 

 

 

Why well-known preventive measures aren’t common practice

Why don’t more people eat healthy diets, get enough exercise, refrain from smoking and drinking too much alcohol, and generally follow practices that would reduce the likelihood of cancer and other chronic illnesses? There are several reasons. First, physicians fail to
convey information about preventive care to their patients, for many reasons: they may not be trained or know enough to do so, they don’t have time, they aren’t reimbursed adequately for time spent urging preventive care, and after hearing conflicting professional recommendations may be skeptical about whether they work. Second, many people don’t know about preventive measures or how to implement them personally. This lack of understanding means people feel little incentive to temper their eating habits or alter their behavior. 

In some communities, including many parts
of DC, the nutrients recommended by
the National Cancer Institute and other
organizations may not be readily available as affordable staples in local food markets. And heavily outweighing public messages about healthy eating is the saturation advertising and pervasive marketing (especially to the young) of heavily processed foods and beverages low in nutritional value and high in fats, sugars, and calories—as well as tobacco companies’
continued subtle advertising to the young. Working parents, short on time, may find it
difficult to cook fresh meals for their families, and instead rely on fast food and processed foods.  Finally, the elimination of some physical education classes in many grades and schools has reduced emphasis on physical activity.

 


Goals, Objectives, and Strategies

GOAL: Reverse the trend toward obesity and overweight by increasing physical
activity and the consumption of fruits and vegetables and by reducing caloric intake among DC residents.

Objectives:

1) Reduce the prevalence rate of obesity among DC adults to 15% by 2010.

2) Reduce the prevalence of overweight adults to 40% by 2010.

3) Reduce the prevalence rate of overweight and obese children to 5% by 2010.

4) Increase to 60% the prevalence rate of adults who engage in regular, moderate
 physical activity for at least 30 minutes a day at least five days a week by 2010.

5) Increase to 40% the prevalence rate of high school students who engage in
 moderate physical activity 30 minutes or more, five or more days a week by 2010.

Strategies:

By January 2008, develop and maintain an intervention clearinghouse that encourages
collaboration among partners; provides resources to program planners and resources to
the public about nutrition, physical activity, and reduced cancer risk; and provides sample ordinances, organizational initiatives, and strategies.

Develop a community-based volunteer cadre to counsel families on health education and
preventive measures for cancer and other diseases.

Develop culturally appropriate materials and promote prevention activities through community educational forums, the media, the DC government, employers and other vehicles.

Include prevention information in all DC forums that address cancer issues.

Join or supplement the efforts of other local organizations interested in controlling obesity, such as the American Heart Association and American Diabetes Association.

Through the Mayor’s Council on Physical Fitness, implement school and work-based
programs for interventions designed to improve healthy eating habits and physical activity, especially among children, teenagers, and young adults.

Encourage employers to adopt programs that promote physical activity, such as onsite
exercise facilities and subsidies for gym or athletic club memberships.

Support Board of Education efforts to provide healthy, well-balanced meals to students in grades K-12, and to encourage good life-long eating behaviors.

Decrease the availability and marketing of foods and beverages of low nutritional value in schools and increase the availability of nutritious food products.

Through professional organizations, conduct educational programs so that physicians can promote the benefits of prevention practices to their patients.


References

Block G, Patterson B, Subar A. Fruit, vegetables, and cancer prevention: a review of the epidemiological evidence. Nutr Cancer. 1992;18:129-

Bowman SA, Gortmaker SL, Ebbeling CB, Pereira MA, Ludwig DS. Effects of fast-food consumption on energy intake and diet quality among children in a national household survey. Pediatrics 2004;113:112-118.

Calle E, et al, Overweight, obesity and mortality form cancer in a prospectively studied cohort of US adults. New England Journal of Medicine 2003;338:1625-1638.

Centers for Disease Control and Prevention. Trends in Intake of Energy and Macronutrients – United States 1971-2000. MMWR 2004;53:80-82.

Day GL, Blot WJ, Shore RE, McLaughlin JK, Austin DF, Greenberg RS, Liff JM, Preston-Martin S, Sarkar S, Schoenberg JB. Second cancers following oral and pharyngeal cancers: role of tobacco and alcohol. Journal of the National Cancer Institute. 1994;86:131-137.

Flegal K, et al. Prevalence and trends in obesity among us adults, 1999-2000. Journal of the American Medical Association.
2002; 288:1723-1727.

Heber D. Vegetables, fruits and phytoestrogens in the prevention of diseases. Journal of Postgraduate Medicine.
2004;50:145-149.

Lew EA, Garfinkeld L. Variations in mortality by weight among 750,000 men and women. Journal of Chronic Disease. 1979;32:563-576.

Ogden C, et al. Prevalence and trends in overweight among u.s. children and adolescents, 1999-2000. Journal of the American Medical Association. 2002; 288:1728-1732.

Smith-Warner SA, Spiegelman D, Yaun SS, van den Brandt PA, Folsom AR, Goldbohm RA, Graham S, Holmberg L, Howe GR, Marshall JR, Miller AB, Potter JD, Speizer FE, Willett WC, Wolk A, Hunter DJ. Alcohol and breast cancer in women: a pooled analysis of cohort studies. Journal of the American Medical Association. 1998;279:535-540.

Steinmetz KA, Potter JD. Vegetables, fruit, and cancer. I. Epidemiology. Cancer Causes and Control. 1991;2:325-357.

Thomas DB. Alcohol as a cause of cancer. Environmental Health Perspective. 1995;103 (Suppl 8):153-160.

United States Department of Agriculture, Agricultural Research Service. Food and Nutrient Intakes by Individuals in the United States by Sex and Age, 1994-1996. Nationwide Food Surveys Report No. 1998; 96-2.

U.S. Department of Health and Human Services. The Surgeon General’s Report on Nutrition and Health, NIH Publication No 8850210. Washington DC, U.S. Printing Office, 1988.

 


Smoking-Related Cancers

 

Facts in brief

Text Box: When states are ranked for mortality rates, DC ranks highest for deaths from
   all smoking-related cancers—for both men and women
(see Table 1). The high
   mortality rates for these cancers may help explain DC’s high overall death rate
   from cancer.

Of the roughly 650 cases of smoking-related cancers a year in the District, about
   400 are lung cancer. Most lung cancers (80 to 90% of cases) are attributable
   to smoking. As many as 75% of oral cavity cancers are probably attributable to
   smoking. Cancers of the lung, larynx, oral cavity and pharynx, esophagus,
stomach, pancreas, bladder, and urinary tract occur more often in smokers
than in nonsmokers.

The lung cancer mortality rate for Black males in DC is similar to the Black rate nationally, but the rate for White males in DC is only 64% of the national rate for White males. In fact, for both White men and women, DC has the lowest lung cancer mortality rate of all states. This fact explains why the lung cancer ranking for the combined races in DC is closer to the average for the United States . However, the very high mortality for all other smoking-related cancers in DC overwhelms the lower rate for the more frequent lung cancer and results in DC leading the nation in mortality for all combined smoking-related cancer sites. 

DC’s Black males carry the heaviest burden of combined smoking-related cancers. The 5-year incidence rates for these cancers is about 50% higher in DC’s Black males than in the same race/gender group nationally. The rate in DC’s Black women is only slightly higher than rates for Black women nationally. The incidence rates of the other smoking-related cancers in White men and women in DC are slightly lower than the national rates.

In comparison with national Surveillance, Epidemiology and End Results (SEER) data, the incidence rates for smoking-related cancers in DC Black males show a greater excess than do the mortality rates according to data from the North American Association of Central Cancer Registries (NAACCR), suggesting that the high mortality ranking for DC is due to the cancers’ more frequent occurrence rather than poorer survival rates after onset of cancer. The same conclusion can be reached for White males and females but not for Black women.

The incidence rates for these smoking-related cancers comparing Black and White males within DC show even greater differences than comparisons with national rates. Rates for
DC Blacks are 2-2.6 times higher than for DC Whites. Black women living in DC also have
incidence rates that are 1.8 times higher than those for White women living in DC. The
disparity by race in the risk of these cancers for both sexes is greater in DC than in the nation.

Excesses in risk for smoking-related cancers in DC’s Black males compared with other race/gender groups in DC begin as early as ages 35-44. Thereafter, these differences rise rapidly.


The risk for various cancer sites in DC Black males is 2 to 8 times higher than for other
groups by ages 55-64, according to NAACCR data.

The higher incidence of smoking-related cancers in DC’s Black population is not attributable to DC’s urban characteristics. DC rates are higher than rates in Atlanta , a comparable East Coast city with a large Black population and minimal heavy industry.

Mortality rates for the combined smoking-related cancers for Blacks in DC are among the highest in the country, whereas the same rates for Whites are among the lowest—which means there is a huge disparity in rates by race in DC.

Since Black males in DC are at higher risk than other racial/ethnic groups for smoking-
related cancers, the goal of any smoking control program in DC should be to reduce the
proportionate number of Black smokers to a level similar to that for Whites.

The rates of smoking-related cancers are almost twice as high in some wards compared to others. These differences in risks by ward might suggest some specific areas of DC where interventions are needed.

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Smoking-related cancers in DC


Inequality is the most striking feature of
incidence and mortality rates for smoking-related cancers in the District. Mortality rates from lung cancer are close to the U.S. average
for all DC residents compared with U.S. residents generally. However, for the combined smoking-related cancers occurring in the aerodigestive system (lung, larynx, oral cavity, esophagus and stomach), as seen in table 1, DC ranks first or second in the nation in mortality rates for both men and women. Mortality rates can reflect not only differences in what causes the disease but also differences in
access to health care and possibly differences in responses to treatment.
The fact that the

 

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 differences in incidence are much greater than the differences in mortality in comparing rates for Blacks and Whites suggests that the major reason for the higher excess mortality in DC in Blacks is the greater frequency of disease in this group. The goal of a smoking-related program for cancer control in DC should aim at reducing this racial disparity.

The incidence rates of lung cancer and other smoking cancers by ward or geographic area and gender in DC show major differences (see Table 2). For example, lung cancer rates in males are higher in Wards 1, 4, 5, 6, 7, and 8 than for males in Wards 2 and 3. Lung cancer and other smoking cancer rates are not always highest in the same wards, however, nor do the highest

 

 

 

 

 

 

 

 

 

Text Box: wards necessarily demonstrate the same excesses for men and women. Ward 3 has the lowest rates for almost all cancers for both men and women. No single ward has the highest rate for all of the cancers, despite the fact that these cancers all have smoking as a unifying risk factor. (All data represent an analysis for a five-year period to stabilize the rates by ward).

Survival

Survival rates from smoking-related cancers are generally very poor. The 5-year survival rates from these cancers (except for larynx and oral cavity cancers) range from 9% to 22%. Even oral cavity and pharyngeal
cancers, with survival rates as high as 60%
in the White population, require extensive
surgery, which is often disfiguring, thereby limiting social interactions and reducing
quality of life.  The U.S. data indicate that survival following these cancers is generally poorer for men than it is for women and
poorer for Blacks than for Whites. Survival is particularly poor for Black males. Although options for screening are limited for many of these cancers, head and neck cancers, the commonest of smoking cancers other than lung,

 

 

 

are amenable to screening (see separate chapter on the subject).

The health burden from smoking

The health burden from smoking is not
confined to cancer. Where there are high rates of smoking, excesses in mortality and
hospitalizations for cardiovascular disease, stroke, and chronic obstructive respiratory
disease are expected. The respiratory
problems in smokers will also result in lost work time and poor quality of life, because
of restricted activity. In women, the burden of smoking is often seen in poor reproductive performance, including infants born prematurely or small for their gestational age.

The burden from smoking is also borne by individuals who live or work with smokers
and are passively exposed to smoke. This environmental contamination increases the risk of lung cancer, heart disease, and other conditions. Reducing smoking rates brings about a fairly immediate reduction in the health and cost burden from some major diseases, whereas the effect on cancer rates may be delayed for 10 to 20 years. Any program that reduces smoking rates will reduce health costs from several diseases, many of which occur with high frequency and high cost.

Risk factors for lung cancer

Several kinds of occupational and environmental exposure have been associated with the risk of lung cancer, but the factor that explains 80 to 90% of cases is cigarette smoking. The risk of lung cancer is reported to be 10 to 20
times higher in smokers than nonsmokers, depending on how long they smoked and how many cigarettes a day they consumed. Black men have higher incidence and mortality rates from lung cancer, are younger at age at
diagnosis, and have worse chances for
survival than White men.

 

 

 

While direct exposure to tobacco smoke is
the most important risk consideration, any
exposure to tobacco smoke carries a risk. Passive exposure to secondhand smoke has been estimated to increase the risk of lung cancer by about 25%. The more cigarettes smoked, the greater the risk to nonsmokers exposed to the smoke. Exposure to environmental tobacco smoke (ETS) is suspected to increase women’s risk of heart disease and children’s risk of respiratory conditions such as asthma attacks, especially in children under the age of 10. In a population with smokers, nonsmokers’ health may be damaged the same way indirectly as smokers’ health is damaged directly. Reducing the number of smokers in DC will reduce not only the direct effects of tobacco on smokers but also will reduce exposure of non-smokers to environmental tobacco smoke. 

Other factors that have been associated with a risk of lung cancer are radon in homes, other environmental radiation, and several industrial chemicals, such as coke oven gas and metals from chromium refining. None of these factors should play a major role in lung cancer risk
in DC.

Risk factors for other smoking-
related cancers

For the other smoking-related cancers,
smoking represents an important risk factor
but not the only one. Tobacco is a major and independent risk factor for cancers of the larynx, oral cavity and pharynx, stomach, and esophagus. For all these cancers, British doctors have demonstrated a sevenfold increased risk for smokers over nonsmokers; heavy smokers had 15 times the risk of nonsmokers. Several studies have shown smokers to be at 3 to 13 times higher risk of oral cavity and pharyngeal cancers than nonsmokers.  

 



 

 

Current smoking levels in DC

Historically, Blacks as a race reportedly start smoking later than Whites and smoke fewer cigarettes, but this pattern may be changing.
According to the Behavioral Risk Factor Surveillance System (BRFSS) (see Table 3), smoking rates in 2003 are higher for Blacks in DC and in the United States than for Whites. However, since DC has a population of African immigrants who smoke, the increase in
smoking reported by Blacks may be attributed to the African immigrant and/or African
American population.

The reported rate of smoking among
Hispanics in DC is higher than the U.S. rate
for Hispanics.

The rate for smokers in DC with low education levels is 43% higher than the overall DC
smoking rate and 11% higher than the U.S. rate for smokers with low education. The high rate for smokers with little education suggests that the DC smoking rate may be associated with low-income residents, which could
explain some of the disparity in lung cancer rates by race.

Preventing smoking-related
cancers

Smoking cessation has been the main focus in reducing tobacco-related cancers, but the ideal primary prevention strategy is to keep people of all ages from starting to smoke in the first place—because tobacco is one of the most addictive drugs. Of course, to stop smoking at any age will in the long run reduce the risk of smoking-related cancers. The
benefits from smoking cessation not only
reduce cancer risks but also may be felt
more immediately and more dramatically in terms of reduced risks of cardiovascular
disease and reproductive problems.

Secondary prevention through screening or early detection is important only for oral cavity

 

 

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cancers. For the other smoking-related
cancers, no practical screening programs
have been developed. . 

 

 

Aims of a DC smoking program for
cancer control

Any anti-smoking program in DC should aim to do four things:

Prevent the initiation of smoking.

Reduce the number of current smokers

Decrease exposures to secondhand smoke

Reduce the racial disparity in smoking-
related cancers by providing effective
smoking-cessation programs for all races.

Each of these aims will demand programs with slightly different emphasis but the programs should overlap as part of an integrated community-based plan that includes all five objectives below. Each objective must be
considered separately but the programs for
all five objectives should be integrated.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Funding for tobacco control in DC

To date, the District of Columbia has spent none of the $57.4 million tobacco-generated
revenue it has received from the tobacco settlement payments and tobacco excise taxes for tobacco control and prevention. The District opted to securitize part of its settlement payments in exchange for a lump-sum payment to repay existing long-term debt. The Centers for Disease Control and Prevention has set minimum expected levels for states to spend on tobacco control and prevention. For DC, the minimum expectation is $7.5 million annually.
The District ranks worst of all states in the amount and percent of tobacco settlement funds it has spent on tobacco control and smoking prevention.

To DC’s credit, the tobacco excise tax is $1.00
per pack. California , Massachusetts , and  Canada have proven that there is a direct relationship between increasing the tobacco excise tax and reducing tobacco use. Sadly, though, the revenue from the tax has not been appropriated for programs to prevent or reduce tobacco use.


Goals, Objectives, and Strategies

GOAL: Reduce mortality from smoking-related cancers in the District of Columbia .

Objectives and strategies:

1) Reduce the level of smoking among high school students from 13% to 10% by
 the year 2010.
   

Initiate anti-smoking programs and smoking cessation programs in all high schools. Use programs similar to current DC programs and adapt programs used successfully elsewhere. Programs for smoking cessation must be racially and culturally appropriate and should  involve both schools and other points of contact (such as youth centers, family planning clinics, pregnancy clinics, and maternal and child health clinics that see youths under 20).

Consider new approaches to reaching young smokers, possibly using a “cluster” approach that engages youths’ parents and peers.

Consider an increase in the cigarette excise tax in 2007.

2) Reduce the level of smoking in current Black and Hispanic smokers and those
 with low levels of education by 25% by the year 2010.

Establish a smoking cessation quit line for DC youth and adults that will address the needs of a multilingual and culturally diverse population. Include counseling and pharmacotherapy components.

Target promotion of the cessation quit line to specific racial, ethnic, and geographic
populations.

Launch a targeted media blitz against smoking.

Educate professionals about their importance and effectiveness in persuading smokers
to stop.

3) Reduce general exposure to secondhand smoke by creating a smoke-free
 environment in all public places by the year 2006.

Advocate for legislation that bans smoking in all public places.

4) Reduce racial disparities in smoking prevalence.

The minimum objective for DC—a thread running through the previous three objectives—should be to ensure that DC meets tobacco goals for Healthy People 2010 (Reduce
adult smoking to 18.5%) and meets CDC’s recommended level of funding for anti-smoking activities ($7.5 million annually).


 


References

Barnoya J, Glantz S. Association of the California tobacco control program with declines in lung cancer incidence. Cancer Causes Control 2004;15:689-695.

Chao A, Thun MJ, Henley SJ, Jacobs EJ, McCullough ML, Calle EE. Cigarette smoking, use of other tobacco products and
stomach cancer mortality in US adults: The Cancer Prevention Study II.
Int J Cancer 2002;101:380-389

Dragnev KH, Stover D, Dmitrovsky E; American College of Chest Physicians. Lung cancer prevention: the guidelines. Chest 2003;123(1 Suppl):60S-71S.

Ginsberg RJ, Vokes EE, Rosenzweig K. Non-small cell lung cancer, in Cancer, Principles and Practice of Oncology, eds DeVita VT Jr, Hellman S, Rosenberg SA, 6th ed, 2001, pp925-983, Lippincott, Philadelphia.

Green PM, Davis MA . Lung cancer in African-Americans. J Natl Black Nurses Assoc. 2004;15:54-60.

Heloma A, Nurminen M, Reijula K, Rantanen J. Smoking prevalence, smoking-related lung diseases, and national tobacco control legislation. Chest 2004;126:1825-1831.

Leistikow B. Lung cancer rates as an index of tobacco smoke exposures: validation against black male approximate non-lung cancer death rates, 1969-2000. Prev Med 2004;38:511-515

Mattson ME, Pollack ES, Cullen JW. What are the odds that smoking will kill you? Am J Public Health 1987;77:425.

O’Brien K, Cokkinides V, Jemal A, Cardinez CJ, Murray T, Samuels A, Ward E, Thun MJ. Cancer statistics for Hispanics, 2003. CA Cancer J Clin. 2003;53:208-226

Seltzer V. Smoking as a risk factor in the health of women. Int J Gynaecol Obstet. 2003;82:393-397.


Head and Neck Cancers

 

Facts in brief

Text Box: Oral cavity and pharynx cancers occur 1.7 times more frequently in Black males in DC than in Black males countrywide. (Local and national incidence rates in White males and in women of both races are similar.) Black males in the District are 2.4 times more likely than White males to be diagnosed with these cancers.

Black males with oral cancers have only half the chance White males have of surviving for 5 years. The poorer survival rates of Black males are partly due to their cancers being diagnosed at a more advanced stage                                                than those of White males.

Incidence rates of cancer at each site in the oral cavity are low but the combined rates represent about 40% of all other smoking-related cancers, except lung cancer, in Black males. The higher rates of cancer in Black males appear to be concentrated in lesions of the tongue, the floor of the mouth, the oropharynx, and the hypopharynx. Lesions at many of these sites would be visible on direct examination of the oral cavity.

The age-specific rates of oral cavity cancers are higher in Black males beginning at ages 35–44, and the rates for Black males increase more rapidly than for other race and gender groups. The rates peak at ages 55–64, when oral cavity cancers are 2.5 times more likely
for Black males in DC than for White. For Black males in DC, the rate of oral cavity cancer
declines after age 64, differing from other smoking-related cancers (including lung and
stomach cancers), which generally show a gradual increase in risk extending past the age
of 75. This may suggest other risk factors for these cancers besides smoking or other
population differences.

Ward 3 has the lowest rate for oral cavity cancers in males. The range of rates by ward differs 4.6-fold. Some of the variation is due to differences in racial distribution by ward.

Patients with oral cavity cancers have a better survival rate than patients with smoking-related cancers at other sites, such as the lung, esophagus, and stomach. However, the treatment
for this cancer may disfigure the patient, leading to a diminished quality of life.

Patients with a first cancer of the oral cavity or pharynx have a 15 to 20 % chance of having
a second new cancer in the same area or in the larynx, lung, or esophagus.


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Cancers of the head and neck, including
tumors arising in the oral cavity and pharynx, are associated with smoking.

Risk factors

Smokers have a 3- to 13-fold higher risk of oral cavity and pharynx cancers than nonsmokers.

 

 

Other factors, such as the use of smokeless tobacco products, also play a role in oral cavity cancers. Data are not available on adult use of smokeless tobacco in DC. According to national data for 2003, 5% of high school students in DC use smokeless tobacco.


Risks for oral cavity cancers double in heavy drinkers, compared with those who abstain from alcohol or are light drinkers. Moreover, studies suggest that combined exposures to smoking and heavy drinking in the population may increase the risk of oral cancer to higher levels than the added risks from each
substance alone. Exposure to both heavy drinking and smoking increases the risk almost 80-fold while the risk from heavy smoking alone may be only 17-fold and the risk from heavy drinking alone only two-fold. Because the two exposures often occur together, most of the cancers will be related to both risks.

Differences in diet are thought to influence the risk of oral cancers. In fact, Chinese people from certain areas of China who eat salted fish have an especially high risk of nasopharyngeal
cancers. Exposure to selected chemicals, such as formaldehyde and methyl ethyl ether, may increase the risk of selected sites of pharynx, nasopharyngeal and hypopharynx cancers.

Preventing oral cancers

Because oral cavity cancers are related both to cigarette smoking and smokeless tobacco products, campaigns encouraging people never to use the products and programs
helping people stop using them could both
be effective.

Oral cancer patients have a 15% risk of
developing a second cancer of the head and neck or in the lungs—a much higher risk of second cancers than for other cancer sites.
Many deaths from head and neck cancers are the result of second cancers. Many of these second lesions occur in the oral cavity or pharynx but may also occur in the larynx, lung, or esophagus. The risk of developing some second cancers might be prevented or the
effects modified by changing patients’
smoking or drinking habits and by early
detection through screening.

 

 

 

Two factors—the high probability of second cancers and a risk for combined exposures that is greater than additive—strengthen the impact of reducing smoking. Where there is
a synergistic effect between two common exposures and especially if the behaviors
frequently occur together, reducing the
exposure to either factor will greatly reduce
the risk of the cancer. Early detection of a
second cancer, or even of premalignant
lesions, may improve the patient’s chances
for survival. Secondary prevention programs could be successful in reducing both
advanced oral cancer lesions and deaths. They would focus on detection of both
precancerous lesions and early-stage disease. Except for pharynx cancers, common sites should be visible on clinical examination.

Early detection is particularly important in
oral cancer prevention because survival is significantly improved if the lesions are small at diagnosis and the extent of surgery may be less. Since surgery for advanced head and neck cancers is extremely deforming, the
patient’s quality of life could be improved
with less radical surgery. Although cancer organizations may not suggest screening
programs for all head and neck cancers
because the cancer is relatively rare, it is
important to add oral cavity screening to
routine clinical examinations, especially by both dental and medical practitioners, and to focus screening programs on high-risk groups.

Secondary prevention would include a
program to teach both physicians and dentists to look for early lesions in the oral cavity and to provide appropriate care for leukoplakia and erythroplakia. The professionals could train their patients to perform self-examination for these lesions. The white or reddish raised plaques found on oral mucosa are often a precancerous condition.

 

 

 

Dentists may perform oral cavity screening routinely but older populations often do not use routine dental services so it is important to train physicians to perform the screening—especially for the elderly, who often see medical doctors for chronic health problems. Physicians may also need to be reminded of the high risk of second primaries of the oral cavity or pharynx in patients with an original primary cancer of the aerodigestive tract. Freestanding oral cancer screening programs are often underused. Primary prevention programs for smoking cessation can be added to these screening programs to enhance their effectiveness. Screening programs might be targeted at high-risk populations such as men in jails and halfway houses and other sites with many high-risk occupants who have had little contact with medical or dental services before living in such group facilities.

Signs and symptoms of head and
neck cancer

The most common symptoms of head and neck cancer are listed below. Usually, only one sign or symptom is present.

An ulcer or sore area in the head or neck that does not heal within a few weeks

Difficulty in swallowing, or pain when
chewing or swallowing

Trouble with breathing or speaking, such
as persistent noisy breathing, slurred speech or a hoarse voice 

A swelling or lump in the mouth or neck

Pain in the face or upper jaw.


Goals, Objectives, and Strategies

GOAL 1: Reduce the mortality rate in DC from cancers of the head and neck by 10%.

GOAL 2: Reduce the incidence of invasive cancers of the head and neck  in DC
by 10%.

Objective: Increase to 50% the proportion of head and neck cancers detected at the local stage for both men and women by 2010.  

Strategies:

Educate dentists, physicians, and other health care providers about screening all patients, especially those who smoke, for early signs of head and neck cancer.

 

Through community, church-based, and work-based programs inform people about  the
risk factors and the early signs and symptoms of head and neck cancer and the need for screening, especially in a smoker or heavy drinker of alcohol.

 

References

Castigliano SG. Influence of continued smoking on the incidence on second primary cancers involving mouth, pharynx, and larynx. J Am Dent Assoc 1968; 77:580-585.

De Stefani E, Correa P, Oreggia F, Leiva J, Rivero S, Fernandez G, Deneo-Pellegrini H, Zavala D, Fontham E. Risk factors for laryngeal cancer. Cancer 1987;60:3087.

Gerson SJ. Oral cancer Crit Rev Oral Biol Med. 1990; 1:153-166.

Greene VA. Underserved elderly issues in the United States: burdens of oral and medical health care Dent Clin North Am. 2005; 49:363-376.

Hunter KD, Parkinson EK, Harrison PR. Profiling early head and neck cancer. Nat Rev Cancer. 2005;5: 127-135.

Licciardello JT, Spitz MR, Hong WK. Multiple primary cancer in patients with cancer of the head and neck: second cancer of the head and neck, esophagus and lung. Int J Radiat Oncol Biol Phys 1989;17-467-476.

McGuirt W, Matthews B, Koufman J. Multiple simultaneous tumors in patients with head and neck cancer: a prospective, sequential panendoscopic study. Cancer 1982;50;1195-1199.

Morton RP, Hay KD, Macann A. On completion of curative treatment of head and neck cancer: why follow up? Curr Opin Otolaryngol Head Neck Surg. 2004;12:142-146.

Russo A, Crosignani P, Berrino F. Tobacco smoking, alcohol drinking and dietary factors as determinants of new primaries among male laryngeal cancer patients: a case-cohort study. Tumori 1996;82:519-525.

Sudbo J, Samuelsson R, Risberg B, Heistein S, et al. Risk markers of oral cancer in clinically normal mucosa as an aid in smoking cessation counseling. J Clin Oncol. 2005; 23:1927-1933.


Breast Cancer

 

Facts in brief

dc Among women, breast cancer is the second leading cause of cancer-related deaths nationally, after lung cancer. Nationally, it is the most commonly diagnosed non-skin cancer among women, accounting for nearly one-third of all cancers diagnosed. Over her lifetime, a woman has a one-in-seven chance of developing breast cancer.

Almost 80% of breast cancers are diagnosed in women aged 50 and older. More than half of breast cancers are diagnosed in women aged 65 and older.  Women 65 and older have a significantly higher mortality rate (148.9) than women 64 and younger (19.8).

Roughly 80% of women diagnosed with breast cancer have no known risk factors.

 

Nationally, White women have the highest incidence rate (140.8. cases per 100,000 women), followed by Black women (121.7), Asian/Pacific Islander women (97.2), and Hispanic women (89.8).

However, Black women have the highest mortality rate nationally (35.9 deaths per 100,000 women), followed by White women (27.2), Hispanic women (17.9), and Asian/Pacific Islander women (12.5).

Between 1992 and 2000 the incidence rate for Black women remained the same. However, Black women were more likely than White women to be diagnosed with large tumors (larger than 5.0cm).

White women have a higher incidence of breast cancer after age 42; Black women have a slightly higher incidence rate before age 42. 

Incidence rates have remained relatively stable, increasing only 0.4% from 1987 to 2000.
Mortality rates declined 2.6% annually from 1992 to 2000—but the decline was twice as great for White women as for Black women.

About 10% of women who are carriers of the BRCA1 or BRCA2 gene develop breast cancer.

The District has the highest breast cancer mortality rate in the country (at 37.3 per 100,000 women).

In 2005 an estimated 520 women in the District will be diagnosed with breast cancer and
100 will die of the disease.

The incidence rate in DC (143.3), the fifth highest among all states, is considerably higher
than the national average (132.2).

Men can get breast cancer, but male breast cancer is rare (1,300 cases per year).

 


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Breast cancer is the most frequently diagnosed cancer among District women and the second most frequently diagnosed cancer among all District residents. The incidence rate is highest in Ward 2 (224.3 per 100,000 women),
followed by Ward 3 (173.0), as Table 1 shows.

The mortality rate from breast cancer is the third highest cancer mortality rate in the District. Ward 2 has the highest breast cancer mortality rate (48.8), followed by Ward 5 (41.7), as Table 2 shows.

Research has documented treatment
differences between Black and White women. Many researchers attribute the delayed
diagnosis of breast cancer in many Black women to a lack of health insurance or
limited access to mammography, although there is some indication that cultural beliefs about health care and socioeconomic factors, such as income and education, may explain some of this disparity. But Black women, especially those

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younger than 45, also develop more aggressive tumors than White women. Those aggressive tumors are difficult to treat and often present at a late stage. Mutations in the p53 tumor suppressor gene, which are associated with poorer outcomes, are more likely to occur in Black women and might make chemotherapy treatment less effective.

Risk factors

Modifiable risks

Alcohol. Studies have shown the risk of breast cancer to increase slightly with increased alcohol consumption.

Diet and obesity. Many cohort studies have found that obesity increases the risk of postmenopausal women developing breast cancer.

Hormonal therapy. Studies suggest that reproductive hormones promote the growth
of some cancers. Recent use of hormone (estrogen) replacement therapy (HRT) has been shown to increase the risk of breast
cancer  (the longer the period of HRT, the greater the risk).

Nonmodifiable risks

Text Box: Breast cancer is the most frequently diagnosed 
cancer among District women and the second most frequently diagnosed cancer among all District residents. Age. The risk of developing breast cancer
increases with age, for both men and women. Most breast cancers occur in women over the age of 50; the risk is especially high for women over the age of 60.

Family history of breast cancer. Only 10% of women who develop breast cancer are genetically
predisposed to developing the disease.
Mutations in two genes (BRCA1 and BRCA 2) account for nearly half of these inherited forms of breast cancer. In addition, women who have two or more first-degree relatives (mother, sister, aunt) with breast cancer diagnosed
at an early age are at increased risk for
developing the disease.

Hormonal history. Women with an early
onset of menstruation (before age 12) are
at higher risk of developing breast cancer. In general, breast cancer risk declines 10% to 20% for each year menarche was delayed. Epidemiological studies have consistently demonstrated that late onset of menopause (age 55 and over) is associated with greater risk of breast cancer.

Childbirth history. Women who experience more pregnancies are at decreased risk, and women who bore their first child when they were 20 years old or younger have about half the risk of women who completed their first full-term pregnancy at age 30 and over. Women who never have children or have their first child after age 30 are at slightly increased risk.

 

 

 

Sexual orientation. When cultural
comparisons are made, lesbian women
appear to be at higher risk of breast (and
cervical) cancer because of delayed
screenings and higher rates of alcohol consumption, tobacco use, obesity, and
never having given birth to a viable infant. 

Ways to reduce the
incidence of breast cancer

Certain actions may lower (but not eliminate) women’s risk of developing breast cancer. Lifestyle changes that may help reduce women’s risk of developing breast
cancer include limiting alcohol consumption,
eating a low-fat diet, breastfeeding their
infants, and increasing physical activity. In the District of Columbia :

Nearly 30% of women 18 and older report engaging in no physical activity.

More than half of adult women in the District, and 68% of Black women, are considered overweight (with a body mass index greater than 25.0). Rates of obesity continue to increase.

DC residents with only a high school
education have overweight rates over 70%.

Research has shown that tamoxifen and other agents can reduce the risk of breast cancer in women who are at high risk for developing the disease, and the risk of recurrence in women who have already had breast cancer. These agents do have side effects.

Prophylactic mastectomy is an option
available to women with moderate to high risk of developing breast cancer in their lifetime.

 

 

 

 

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The procedure can reduce the risk by 90% in women who are at moderate to high risk. However, this is a drastic procedure and should be considered very carefully. It is often regarded as an important option for women who carry the BRCA1 or BRCA2 genes or who are at very high risk for breast cancer
because of a strong family history of the
disease.

Ways to reduce deaths from
breast cancer

Screening and early detection. There has been a modest decline in deaths from breast cancer, which has been attributed to successful screening programs and improvements in treatment. Mammography, an X-ray of the breast, detects about 90% of breast cancers in women without symptoms. Often these cancers are too small for health care providers
to feel during clinical breast examination. Mammography screening may identify women who have cancer or precancerous lesions in the breast that require further evaluation, including a biopsy. Results from post-mammography biopsies are non-cancerous in 70

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

to 80% of women. Mammography testing is more accurate in postmenopausal than in premenopausal women. The breast tissue in younger women is denser than that in post-menopausal women, making it more difficult for mammography to detect breast cancer.

Women diagnosed with breast cancer at an early stage, when the tumor is confined to the breast (localized), have a 97% chance of surviving 5 years; when the cancer has spread to the region around the breast, 78%; and when the cancer has spread to other organs, 23%. Table 3 shows data on stage of cancer at diagnosis in District wards.

Although some recent studies have cast doubt on the value of mammography screenings, both the National Cancer Institute and the American Cancer Society firmly support the value of mammography as a means of
detecting breast cancer at an early stage. The American Cancer Society recommends that:

Women get yearly mammograms starting
at age 40.

 

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Clinical breast exam (CBE) be part of a
periodic health exam about every three years for women in their twenties and thirties, and every year for women 40 and older.

Women know how their breasts normally
feel and report any breast change promptly to their health care provider.

Women at increased risk (through family
history, genetic tendency, or past breast
cancer) talk with their doctors about the benefits and limitations of starting
mammography screening earlier, having
additional tests (such as breast ultrasound and MRI), or having more frequent exams.

According to the Behavioral Risk Factor
Surveillance System (BRFSS), although
proportionately more women in DC are getting
recommended mammograms than do so
nationally, 30% of women in the District are
still not being screened regularly for breast cancer (see table 4). Only 69% of women in the District 65 years old and older reported having had a mammogram in the past year, although the incidence of breast cancer increases the most among women in their sixties.

 

 

 

More Black women (72%) are receiving
mammograms than White women (62%) in DC, but only 64% of women with less than
a high school education are receiving
mammograms.

In 2004, the Delmarva Foundation, a quality improvement organization, reported that only 51% of Black women on Medicare (age 65+ and/or disabled) are being screened for breast cancer, compared with 61% nationwide.

Diagnosis. If a palpable mass is present or a mammogram reveals a suspicious lesion, a
biopsy is needed to determine the nature of the lesion, or mass. Three types of biopsy procedure are available: fine needle aspiration, core biopsy, or excisional biopsy. Each has advantages and disadvantages. The type of biopsy required often depends on the mass’s location, size, and visibility on the mammogram.

Treatment. Breast cancer is commonly treated by a combination of surgery, radiation therapy, chemotherapy, and hormone therapy. Surgery is still the first line of treatment, but researchers have found that less extensive, more conservative surgery is just as effective as radical surgery. Now surgeons may remove
only the tumor or only a small part of the breast, especially if the cancer is small. One reason for regular mammograms is to find the small tumors so that extensive surgery is not needed. For large tumors, a simple or more extensive mastectomy may be necessary, but reconstruction of the breast is often possible. In some cases, radiation or hormonal therapy or chemotherapy may be required in addition to surgery. The additional treatment is designed to remove any residual tumor that may have not been visible at surgery.

Selection of therapy is influenced by age, menopausal status, stage of disease, the
tumor’s histologic and nuclear grade, and status

 

 

 

 

in terms of estrogen and progesterone, among other factors. The earlier the breast cancer is diagnosed, the more treatment options women have.

Barriers to reducing the breast
cancer burden

Women’s knowledge, attitudes, and
beliefs.
Some women avoid mammograms out of a belief that screening is unnecessary if the woman is asymptomatic or has no family
history of cancer. Others fear a diagnosis of cancer. One study found that Blacks knew less about cancer and were more fatalistic about it than Whites.

Socioeconomic barriers. Age, poverty, and isolation make it difficult for many women in the District to get either primary care or cancer care. In a city with a high cost of living, 36% of residents are at 200% of the federal poverty level or below. For 30% to 40% of minorities, cost is the reason women report failing to follow up on their physicians’ recommendations. Women also have trouble getting time off from work and finding adequate transportation and child care. English is not the primary language for about 17% of DC residents, and access to language interpreters is limited. Poor literacy, including poor health literacy, makes it difficult for many patients to understand and follow instructions from the doctor or the pharmacy.

Cultural issues between patients and health care providers. Minority and immigrant residents report they do not sense an understanding or respect from physicians who do not share their racial and ethnic heritage. 

Lack of access to health care providers and screening. The waiting time for a
mammogram in DC is now five weeks. For women who have trouble getting time off from work, finding help with child care, and making their way on public transportation to screening
services and clinical breast exams, having to wait

 

 

a long time to be seen is discouraging.
They often lose their motivation and fail to show up for appointments.

There are too few mammography facilities, especially in areas that serve the poor. D.C. General Hospital closed all inpatient services in spring 2001 and some outpatient services, including breast cancer screening. Hadley Hospital and Columbia Hospital for Women, primary providers of mammography and
other breast health services, also went out
of business.

There are insufficient public screening and treatment resources for the medically
underserved through Project WISH, the District’s Breast and Cervical Cancer Early Detection Program.

It is unknown what percentage of women eligible for Project WISH in DC are served. Nationwide Breast and Cervical Early
Detection Programs serve only 10% to
20% of the eligible population. The District government does not supplement federal funding, so Project WISH must designate
most of its funds to serving women aged 50 to 64. There are few other resources in the District to screen women between the ages
of 40 and 49.

Fragmented health care system. In DC,
community health centers have difficulty
finding specialists who will take cases of
medically underserved women who need follow-up and/or treatment after a suspicious mammogram.

Difficulty navigating the health care
system.
Sometimes understanding and
maneuvering through the health care
system (making an appointment, following
pre-appointment instructions, getting to the

appointment, understanding the findings and

 

 

 

instructions from the health care provider and following through on the instructions) can be overwhelming to a person. Especially if a woman faces any of the additional barriers mentioned above, she may not pursue the screening or medical appointment.

Lack of access to rehabilitation and
support services.
Not all women are referred appropriately to rehabilitation services, support
programs, or other cancer care resources.

 


Goals, Objectives, and Strategies

GOAL: Reduce mortality rates from breast cancer in the District by 10%, especially among Black women.

Objectives:    

1) Reduce the incidence of invasive disease in DC by 10% by 2010.

2) Increase the number of women aged 50 through 64 who are screened annually
 by 10% by 2010.

3) Reduce the proportion of unstaged cases to less than 5% by 2010.

Strategies targeted to women:

Partner with community organizations and local breast cancer organizations to bring tailored messages about breast cancer screening to all medically underserved Black women and to women 50 years old and older. Encourage such groups to enlist the help of influential public figures from whom such messages might be more persuasive. Tailored messages should
address myths, fears, and negative attitudes about breast cancer and screening.

Partner with local Centers for Medicare and Medicaid (CMS), AARP, senior service
organizations, and the Department of Motor Vehicles to educate Medicare and Medicaid
beneficiaries about the benefits and coverage for breast cancer screening.

Make information about resources for breast cancer screening, treatment, and support readily available to women.

Strategies involving system-wide change or activities:

Advocate for sufficient city funding for Project WISH to supplement federal funding, so that
the program can reach at least 50% of the women eligible for the program.

Subcontract additional components of Project WISH if management and budgeting for the program are inadequate or unstable.

Develop a system that coordinates and connects community health centers with hospitals to ensure continuity of care regardless of patients’ insurance or payor status.

Implement a patient navigation system in DC to help women connect with appropriate
diagnostic services, treatment facilities, medical appointments, second opinions, and
follow-up examinations.

Expand the mobile mammography screening program, especially for Black women. Such a program could also screen for hypertension, cholesterol, and other diseases.

Strategies targeting health care providers:

Ensure that all appropriate health care providers know about breast cancer screening
guidelines, local resources for screening and treatment of medically underserved women,
and community resources that support screening, treatment, and referral.

Ensure that all appropriate health care providers are trained to provide clinical breast
examinations for women at the appropriate age.

Make a family history of breast cancer a required part of every woman’s medical record.

Encourage physicians to set up effective reminder systems for annual screening of female patients.

Make screening a part of annual physical examinations for all women 50 years old and older.

 

 

References

Agency for Healthcare Research and Quality. Diffusion and Dissemination of Evidence-based Cancer Control Interventions.
Summary, Evidence Report/Technology Assessment: Number 79. AHRQ Publication Number 03-E032, May 2003. Available at http://www.ahrq.gov/clinic/epcsums/canconsum.htm. Accessed April 20, 2005.

Breast Cancer Facts and Figures 2003-2004. American Cancer Society.

Centers for Disease Control and Prevention. Studies on Improving the Use of Breast, Cervical and Colorectal Screening. Guide to Community Preventive Services. Available at http://www.thecommunityguide.org/cancer/screening. Accessed April 15, 2005.

Champion VL, Skinner CS, Menon U, Seshadri R, Anzalone DC , Rawl SM. Comparisons of tailored mammography interventions at two months postintervention. Ann Behav Med. 2002 Summer, 24 (3): 211-8.

Collins KS , Hughes DL, Doty MM, Ives BL, Edwards JN, Tenney K. Diverse communities, common concerns: assessing health care quality for minority Americans. The Commonwealth Fund. Available at www.cmwf.org/publications. Accessed September 30, 2003.

D.C. Literacy Clearinghouse. Literacy Statistics. Available at http://dclearns.org/clearinghouse/stats. Accessed May 16, 2005.       

Love SM, Lindsey K. Dr. Susan Love’s Breast Book. 3rd ed. Perseus Publishing, 2000.

Mandelblatt JS and Yabroff KR. Effectiveness of interventions designed to increase mammography use: A meta-analysis of
provider-targeted strategies.
Cancer EpidemiolBiomarkers Prev 1999; 8:759-767.

Susan G. Komen. (2005). Breast Cancer Needs Assessment of the National Capital Area.

 


Gynecologic Cancers

 

Facts in brief:

Text Box: Gynecologic cancers account for 6% of cancers diagnosed in the District of
   Columbia
each year. Close to 200 cases a year are diagnosed, including about
   50 cases of invasive cervical cancers, more than 40 of ovarian cancer, 70 to 90
   of endometrial (uterine) cancer, and an unknown number of pre-invasive cervical
   cancers.

Death from one gynecologic cancer—cervical cancer—is avoidable. Since the
   introduction of Papanicolaou (Pap) smear screening programs in this country in
   the 1950s, cervical cancer mortality rates have declined by about 75%. Despite
   high rates of disease, cervical cancer mortality has declined in DC as well.

 

DC has the highest rate of cervical cancer in the United States , and the proportion of cervical cancer cases diagnosed in advanced and unknown stages is greater in DC than in the rest of the country (see Figure 1). Nearly all cases (92%) of invasive cervical cancer are diagnosed among minority women. Only Black women in DC have higher than U.S. average death rates from cervical cancer. Yet invasive cervical cancer is a preventable disease. The main reason women are diagnosed after cervical cancer has spread and the main reason they die—is that they have not received a Pap smear. Evidence shows that women are most likely to get a Pap smear if a doctor recommends it.

Endometrial (uterine) cancer is often a curable disease. In 95% of cases there is vaginal bleeding. Women should be alerted to recognize bleeding after menopause as an early warning sign that could lead to earlier diagnosis and the greater likelihood of a cure.

Late diagnosis is also the main reason for the high mortality rate from ovarian cancer, and there are only subtle early symptoms and warning signs that women and health care providers can watch for. In the absence of a screening test, awareness of the disease’s symptoms may help women seek medical care earlier in this cancer’s progress.


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A single intervention could reduce deaths
from cervical cancer. Unfortunately, fewer
interventions exist for the other gynecologic cancers, although new screening tests may be on the horizon. In this chapter we provide information about, and suggestions for controlling, cervical cancer, endometrial
(uterine) cancer, and ovarian cancer in the District of Columbia .

 

 

 

 

 

CERVICAL CANCER

In the diagnosis and treatment of cervical cancer, regular use of Pap smear screening is critical because precancerous changes can be detected and readily treated.  Pap smear screening rates have increased dramatically in the past two decades; well over 80% of women surveyed nationally reported having had a recent Pap test.

Screening rates in the District are on a par with the rest of the country, with 89.4% of DC women reporting having had a Pap smear in

 

 

 

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The past 3 years and 94% reporting they ever had a Pap smear. Despite these high rates, there has been a worrisome decline in the proportion of women reporting a recent Pap smear (see Figure 2). There is some indication that this trend reflects an influx of Latinas, many of whom are emigrating from countries with very high rates of cervical cancer and poor access to screening.

Almost all women with cervical cancer are infected with human papillomavirus (HPV), which is the main cause of this cancer. (Note, however, that although infection with HPV is apparently necessary for cervical cancer to develop, most women infected with HPV clear the infection spontaneously and do not
develop cervical cancer.) Retrospective
reviews of new cases of cervical cancer, or
follow-back studies, consistently report that the majority (45% to 65%) of new cases occur in women who have never been screened or among those whose last test was three or more years before their diagnosis.
Among cases with recent screening, up to one-third of

 

 

 

cases have been interpreted as failure to detect existing precancerous or cancerous lesions, and between 4% and 30% of cases failed to receive timely, or any,
diagnostic evaluation.

Risk factors for cervical cancer

Studies show that several factors increase the risk of cervical cancer. Risky behaviors exert their influence through their effects on the risk of acquiring or maintaining specific strains of infection with human papillomavirus (HPV). Women who are sexually active at an early age, or have multiple sexual partners, are at greater risk of infection. Women who acquire HPV are at greater risk of having that infection
persist to cause cancer if they are older, smoke, are pregnant, are infected with HIV or are otherwise immune suppressed, have severely limited diets (poor in folic acid, vitamin
C, and other micronutrients), or use oral contraceptive pills. Women who are poor and have no health insurance or regular source of health care are at greater risk of dying from advanced cervical cancer because, in that population group, rates of screening, follow-
up on abnormal tests, and definitive cancer treatment are much lower. Women who undergo a complete hysterectomy for conditions other than cancer are no longer at risk of developing abnormal cervical tissue because all cervical tissue has been removed.

In a study characterizing HPV infection among DC women, Hildesheim and colleagues found a 34% prevalence of HPV infection among 400 low-income women with normal Pap smears who were receiving care at publicly funded clinics in the late 1980s. We do not have any more recent data using newer, more sensitive HPV tests, so the rates are probably higher at present. Many of the women among DC’s growing Latino population have recently emigrated from countries in Central and South America that have some of the world’s highest prevalence rates for HPV infection
and cervical cancer. Cervical cancer is the

 

 

 

 

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fourth leading cause of death from cancer in Latinas in the United States . According to SEER 2000 data, Latinas have the highest rates of cervical cancer rates of all U.S.
population groups.

Screening for cervical cancer

Screening for cervical cancer is recommended starting within the first three to five years after the onset of sexual activity or by age 21. After two or three negative annual Pap smears, screening is recommended every two or three years. The American Cancer Society and
the American College of Obstetricians and Gynecologists recommend the FDA-approved HPV DNA test as a reasonable approach to screening women 30 or older, as an alternative to examination alone. If a woman has had more than five to seven normal Pap smears, including a normal Pap smear within the past three years, screening can probably cease after age 65 or 70. Screening is also unnecessary for women who have had a hysterectomy for noncancerous conditions or for women with medical conditions limiting life expectancy to less than five years.

 

 

 

 

 

 

The most important reason that women present with cervical cancer that has already spread or die from this disease is failure to obtain a regular Pap smear. Roughly half of the cervical cancers detected nationally are in women who have never been screened and 10% are in women who haven’t been screened within the last five years. For Pap smear screening to lead to early detection of precursors of cervical cancer or invasive
disease, women must receive regular Pap smear screening, the quality of the smears and their interpretation must be adequate, and when findings are abnormal, follow-up and resolution must be prompt.

Nationally, the main reasons women don’t
get Pap smears include the following: Their
doctor fails to recommend it; they don’t have a regular health care provider, live in an area with few primary care providers, or haven’t had a recent visit; they don’t know where screenings are available or why screening is important; they fear a cancer diagnosis or believe cancer cannot be cured; they want to avoid the
inconvenience, discomfort, or embarrassment of the Pap smear; or they don’t have time.
If they don’t have health insurance, cost is probably also a factor. And cultural beliefs held by new immigrants or other minority groups may also affect whether they seek screening. Similar problems with knowledge, attitudes, and beliefs have been reported as barriers
to follow-up on abnormal screening tests or symptoms of cervical cancer. 

The risk of dying from cervical cancer is
greater in the District’s medically underserved
communities, including southeast DC. Where there are fewer primary and cancer care physicians there will be less patient education about risk factors, fewer recommendations for screening, and less access to treatment. The most common reason for failure to obtain a Pap smear is the health care provider’s failure to recommend it.

 

 

 

 

 

Variations in sensitivity of Pap tests

Text Box: Death from one gynecologic cancer—cervical cancer—
is avoidable. Since the 
introduction of Papanicolaou 
(Pap) smear screening 
programs in this country in the 1950s, cervical cancer mortality rates have declined by about 75%. Despite high rates of disease, cervical 
cancer mortality has 
declined in DC as well. Recent analyses suggest that Pap smears
in general practice vary widely in ability to detect changes in tissue. Sensitivity may vary because of poor exfoliation of cells from the cervix, inadequate sampling by the provider, and/or inaccurate laboratory interpretation. Physicians also vary in their understanding of what makes a smear unsatisfactory. With so much variability in test performance, some women could be classified either false positive or false negative. There appears to be no data summarizing screening quality in the DC area. Adding HPV testing improves detection of true disease.

Follow-up after screening

Black women self-reported comparable or higher rates of Pap smear use than Whites starting in the 1980s, but rates of incomplete diagnostic follow-up and initial
diagnosis at the stage of invasive and
late-stage disease have been consistently higher among Black, Latinas, and other
minority women. Problems with language,
acculturation, and access, as well as fewer years spent in the United States account for low screening rates and late diagnosis among minority immigrant women.

Treatment for cervical cancer

 Women diagnosed before cervical cancer spreads have a dramatically better chance of survival. Two other factors can influence stage-specific survival: the histological (cell) type of cancer and the treatment prescribed. In general, there are two main types of cervical cancer: squamous cell and glandular (adenocarcinoma). In the few studies conducted, there appears to be no difference in histological type in cancers in the DC (compared with

 

 

 

the United States ) that would lead to lower survival rates in DC. But studies show that about 10% of all women diagnosed with invasive cervical cancer receive no cancer-directed therapy or receive inappropriate care. Minority women, older women, and women with distant or unstaged disease are less likely to receive
cancer treatment. We found no studies of
cervical cancer treatment patterns in the
District.

Reaching women and preventing deaths

Invasive cervical cancer is a preventable
disease. Even the highest cervical cancer
rates in the country translate into relatively few women affected (compared with other cancers), but all cases of invasive cervical cancer—especially those arising from lack of screening or adequate follow-up—signal the public health system’s failure to detect and treat this disease at its early, pre-invasive stage. All cases of invasive cervical cancer should therefore trigger a
careful review of missed opportunities for
controlling the disease.

Research indicates that efforts to reduce HPV prevalence, increase screening rates or Pap test sensitivity, or improve compliance with follow-up will all yield significant reductions in cervical cancer incidence and mortality. So will improved treatment. Interventions to increase Pap smear screenings vary tremendously
in effectiveness. Because the levels of HPV prevalence, screening frequency and

 

 

 

 


 


quality, and treatment are largely unmeasured in the District, it is difficult to select a single “best” cancer control strategy. Interventions that have proven effective elsewhere include mailed or telephone reminders to get a Pap smear (which increased Pap smear use by up to 18.8%), using a culturally appropriate lay health worker (which increased use by 18.0%), and offering same-day screening using a nurse-practitioner (which increased screening by 32.7%). Various interventions should be tested and evaluated for effectiveness with
different District populations.

Newer interventions in development may have future applications in DC. For instance, vaccines to prevent infection in women with HPV 16 and 18 are expected to become available in the near future. Immunization would need to occur before the onset of sexual activity. Data on the efficacy of HPV vaccines in males are not yet available. The first clinical trials have shown 100% effectiveness, so this technology is promising.

 

 

ENDOMETRIAL
(UTERINE) CANCER

Endometrial cancer, which develops from the endometrium, the inner lining of the uterus, is the fourth most common cancer in women, after lung, breast, and colon cancer. In 2005 about 40,000 women nationwide will be diagnosed with endometrial cancer; about 7,300 are expected to die of the disease. About 70% of all cases of endometrial cancer occurs in women aged 45 to 74;
only 8% occur in younger women. The chance of any woman being diagnosed with endometrial cancer is about 1 in 40, according to the National Cancer Institute.

After increasing from 1988 to 1998, incidence rates of endometrial cancer leveled off through 2001. The 5-year relative survival rate is 85%, and when this cancer is diagnosed at an early stage—as is the case for most

 

 

 

 

 

women—the 5-year survival rate increases to 96%.
Although this cancer is 40% more common
in White women, Black women are nearly twice as likely to die from it. Survival rates for Whites exceed those for Blacks by at least 10 percentage points at every stage
of diagnosis.

Burden of endometrial cancer in
Washington , DC

In 2002, 84 women were diagnosed with
endometrial cancer, and 31 died of the
disease, as reported in the latest information available from the DC Cancer Registry.

Endometrial cancer mortality rates in DC increased slightly from 1978-2002 but have remained stable in the period 1998-2002. Mortality rates in the District for Black women are higher than those for White women,
and higher than those for Black women
nationwide.

Risk factors for endometrial cancer

According to a recent publication for
physicians from the American College of
Obstetricians and Gynecologists (ACOG) and the Society of Gynecologic Oncologists, the most common cause of endometrial cancer is an excess of estrogen, a female hormone, often found in women who take estrogen
therapy alone after menopause. However, women who take combination birth control pills (estrogen plus progestin) appear to have
a lower risk. Other risk factors include

Not ovulating regularly and often missing menstrual periods

Beginning menstruation before age 12

A history of infertility or never having
given birth

Experiencing menopause late in life

 

 


Use of tamoxifen, an anti-estrogen drug used to treat women with breast cancer

Obesity and/or diabetes

A high-fat diet

Family history, especially for women with the inherited tendency to develop a type of colon cancer called hereditary nonpolyposis colon cancer (HNPCC)

Endometrial hyperplasia (abnormal
thickening of the endometrium)

Breast or ovarian cancer

Prior pelvic radiation therapy.

It’s important to understand that only a small percentage of women who have only one of these risk factors will develop endometrial cancer.

Interventions to decrease the
burden of endometrial cancer

Prevention. Most cases of endometrial cancer cannot be prevented. However, these steps can help lower risk:

Use of oral contraceptives. Taking these
for a long time appears to offer protection
for at least 10 years after a woman stops taking them.

Controlling obesity and diabetes

Eating a diet high in fruits, vegetables and whole grains

Regular exercise.

Screening and early detection. At present there is no early detection test or examination recommended for women without symptoms who are at average risk for this disease. The American Cancer Society recommends that at the time of menopause, women should be made aware about the signs and symptoms of this cancer, especially the importance of seeking immediate treatment for any vaginal bleeding. About 90% of women with endometrial

 

 

 

 

 

 

cancer develop vaginal bleeding or discharge that generally leads to early diagnosis. The Pap test for cervical cancer does not detect gynecologic cancers other than cervical cancer.

Treatment. Treatment for endometrial cancer depends on the type and stage of the cancer
when it is diagnosed and each woman’s overall health. It is important that women with this cancer have their cancers thoroughly and systematically staged to help determine the best course of treatment. Surgery is the most common treatment for endometrial cancer, and in some cases radiation treatment may be recommended. Chemotherapy may sometimes be used, and hormone therapy is also an option for some forms of endometrial cancer.

Follow-up. After treatment for endometrial cancer is complete, monitoring for recurrence should include pelvic examinations every three to four months for two or three years, and
then twice a year thereafter. About 75% of
recurrences are found within the first three years of follow-up; thereafter, recurrence is
less likely.

Barriers to care for endometrial cancer

Barriers include:

The absence of a screening test

Unawareness of the fact that vaginal bleeding or discharge is an early and important
warning sign for this cancer—thereby
delaying diagnosis and treatment

Limited access to specialists, which may mean that initial surgery for this cancer may not produce the careful staging of the
disease needed to determine optimal
treatment

 

 

 



Delays in treatment, inadequate monitoring of the disease during and after treatment, and inadequate support for side effects from treatment because patients are uninsured or underinsured (a recurrent theme).

 

OVARIAN CANCER

Ovarian cancer is the deadliest of gynecologic cancers, accounting for more deaths than any other cancer of the female reproductive system. This cancer, for which there is presently no screening test for the general population, is the fifth most commonly diagnosed cancer among women, ranking second among gynecologic cancers.
Ovarian cancer represents about 3% of all cancers diagnosed in women. Nationally about 22,220 women are expected to contract the disease in 2005, and 16,210 women will die from it.

During 1995-2001, the incidence of ovarian cancer declined at a rate of 0.8% a year, with rates declining fastest in women 65 or older. The incidence of ovarian cancer is 18.1 for Whites (per 100,000 women, age-adjusted to the 2000 U.S. population standard) and 12.0 for Blacks. The mortality rate for Whites is 9.3; for Blacks, 7.6.

In 1995-2000, about 78% of women with ovarian cancer survived one year after diagnosis and, according to the American Cancer Society, the overall 5-year survival rate is 44%. For women diagnosed and treated

 

 

 

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before the cancer has spread outside the ovary, the 5-year survival rate is 90 to 95%. But only 21% of ovarian cancers are found at this early, localized stage.

Burden of ovarian cancer in
Washington , DC

In 2002, the latest data available from the DC Cancer Registry reported that 41 women in the District developed ovarian cancer (see Table 1), and 32 died of the disease.

The disease has a very high rate of recurrence, especially for the great majority of women who are diagnosed with cancer that has spread beyond the ovary. Women in recurrence often undergo years of treatment before a majority succumb to the disease.

Impact of disease stage. Statistics for 1997-2001 show that 58% of Black women diagnosed with ovarian cancer in DC have advanced disease (regional or distant metastases), compared with 45% of White women. Early-stage diagnosis is a strong predictor of treatment success for all women with ovarian cancer.

It is worth noting is that in the District, 24% of Black women and 28% of White women are reported as having “unknown” staging. This suggests either pervasive reporting problems
or a relatively high percentage of surgery on ovarian cancer patients that may not be performed by gynecologic oncologists, the physicians who specialize in treating women with gynecologic cancers.

 

 


Risk factors for ovarian cancer

Age. The risk of ovarian cancer increases with age, especially at or after menopause. About 50% of all ovarian cancers are found in women over 63.

A family history of ovarian cancer. Women with a family history of ovarian cancer have a
higher risk of developing it. Women with a personal or family history of breast and/or colorectal cancers are also at increased risk. Risk may be inherited from either side of the family. However, only about 10% of ovarian cancers result from an inherited tendency to develop the disease. Mutations of the BRCA 1 and BRCA2 genes produce a very high risk of ovarian cancer. Also, hereditary nonpolyposis colon cancer (HNPCC), a syndrome caused by gene mutations, puts people at high risk for colorectal cancer and endometrial (uterine) cancer. While the risk level for ovarian cancer is much smaller with HNPCC than with the BRCA1 and BRCA2 mutation, this genetic mutation does cause 1% of all ovarian
cancers.

Infertility or history of no childbearing. Some research shows that prolonged use of the fertility drug clomiphene citrate, especially without achieving pregnancy, may increase risk for developing ovarian cancer. Also, women who have had no children or who had their first child after age 30 or experienced
menopause after age 50 may have an
increased risk of ovarian cancer, as there appears to be some correlation between the number of menstrual cycles in a lifetime and the risk of ovarian cancer.

Use of estrogen replacement therapy and hormone replacement therapy. Recent information suggests that using estrogen replacement therapy (ERT) increases the risk of developing ovarian cancer, and that the risk increases with continued use. The risk among women who used ERT longer than 10 years was almost double

 

 

 

 

 

 

that of women who had never used it, and the risk tripled among those who used it for 20 years or more.

Interventions to decrease the burden
of ovarian cancer

Prevention. There is no proven way to
prevent the development of ovarian cancer, but steps can be taken to reduce risk. Women with a family history of ovarian cancer
and/or breast cancer may consider genetic testing, surgical removal of ovaries and
fallopian tubes, and other steps that may help decrease risk. Decisions about risk reduction should be made in consultation with family members and health care professionals who can help assess risk and available options.

Increased awareness of symptoms.
Conventional medical wisdom used to be that there were no symptoms of ovarian cancer, but
recent research has documented a clear cluster of symptoms. It is important to teach women
to be aware that a cluster of symptoms—
including back pain, fatigue, bloating, constipation, abdominal pain, and urinary urgency—
may be warning signs when they occur frequently and increase in severity over time.

Screening. There is no reliable screening method for ovarian cancer at present.
Available methods now include a CA-125 blood test and a transvaginal ultrasound for women who have symptoms suggesting ovarian cancer or who are at high risk for the disease. Only about half of women with early-stage ovarian cancer have elevated levels of CA-125, and the test sometimes produces false-positive results. Neither of these tests is intended for general screening and neither is accurate enough to justify use in routine care for women, but a clinical trial is presently under way to determine the effectiveness of this combination of tests for women at high risk.


Development of better screening tests.
At present numerous approaches are being tested to develop a screening test, including studies based on proteomics (the study of cell proteins). It is thought that changes in an
organ caused by the presence of a disease such as cancer may produce detectable changes in the patterns of blood proteins, enabling testers to detect the difference
between cancer and noncancer. Several specific patterns for ovarian cancer have been identified, involving different analysis techniques, but tests need to be validated in clinical trials involving large groups of women before it can be determined if a reliable
screening test is possible using this approach.

Treatment. Treatment for ovarian cancer is generally predicated on the stage of the disease but almost always involves surgery and chemotherapy. The kind of surgery
depends on how far the cancer has spread. Evidence shows that these complex surgeries should be performed by a gynecologic oncologist, a cancer specialist expert in this surgery. These specialists will stage the cancer appropriately and will remove as much of the cancer as possible. Chemotherapy is almost always given to women with ovarian cancer, especially those whose cancer has spread beyond the ovary. In some instances,
radiation therapy or other treatments may
also be recommended.

Support

Access to support during and after treatment is important to women with ovarian cancer, as many cancers recur and women may need support, information, and assistance for years beyond initial diagnosis. Some DC area cancer centers—notably Georgetown University Lombardi Cancer Center and George Washington University Cancer Institute, both in Ward 2—have ongoing moderated support groups specifically for women with gynecologic cancers.

 

 

 

 

 

 

Initial ovarian cancer treatment, including surgery and chemotherapy, often lasts for almost a year, and many women achieving remission will require months beyond the end of treatment to achieve their former energy levels and the abatement of chemotherapy’s side effects. Moreover, recurrence rates are high, and women facing recurrence also face difficult chemotherapy regimens and perhaps additional surgery. Women who are well supported by family, friends, and compassionate employers face a less challenging time than those who are not.

Most ovarian cancer chemotherapy can be given at physicians’ offices, at cancer centers and other hospitals, and, in rare instances, at clinics. Many of the hospitals treating gynecologic cancers are located in Wards 1, 2, 3, and 4 (Howard, George Washington, Georgetown , Sibley, and Walter Reed); Wards 6, 7, and 8 are distant from the area’s cancer centers. Women who rely on public transportation to reach treatment face an
additional burden.

Barriers to care for ovarian cancer

There are several barriers to adequate care of ovarian cancer patients, apart from the fact that there is no reliable screening tool for ovarian cancer. Barriers include:

Not recognizing warning signs and
symptoms.
Lack of awareness of the subtle warning signs of ovarian cancer by physicians and patients can produce a late diagnosis. Moreover, some women erroneously believe that the Pap test also screens for ovarian cancer.

Delayed diagnosis. Some medical
professionals may be unaware that ovarian cancer has symptoms and may misdiagnose women in their care, especially since many of the symptoms of the disease can be confused with other conditions.


Not infrequently women diagnosed with ovarian cancer complain of long waits and of needing to see multiple
physicians to get a correct diagnosis.

Limited access to specialists. Surgery is sometimes performed on women with ovarian cancer by doctors with no specialized training in gynecologic oncology. This results in less-than-optimal surgery and inadequate screening, which may yield inadequate treatment throughout the course of the disease.

Inadequate treatment. For women who are uninsured or underinsured, the District’s clinics and Medicaid may offer the only avenue for getting treatment for ovarian cancer. There is no research documenting these problems
in the District, but anecdotal evidence
suggests that in this environment women may
experience delayed treatments, missed
treatments, insufficient monitoring for disease progression and recurrence, no appropriate treatment for side effects, and insufficient social support. Patients who rely on the District’s Healthcare Alliance system suffer because very few physicians and other health care professionals are willing to treat them because of the Alliance ’s reputation for late and below-cost reimbursement for services and for medications for managing the disease and side effects.

 


Goals, Objectives, and Strategies

GOAL 1: Identify a greater proportion of cervical cancer cases before the cancer has spread beyond the local stage.

Objectives and strategies:    

1) Increase the proportion of women diagnosed at the local stage to 90% by 2010.

Conduct a retrospective review of invasive cases to identify missed opportunities or problems with the quality of care.

Focus resources on identifying and screening women 30+ who have never had Pap smears.

2) Increase the rate of Pap screening to 90% (recent screens) and 97% (ever-screened)
 in all subgroups by 2010.

Survey women to assess knowledge, attitudes, and behaviors and to address barriers to
regular screening. Use a multilingual survey and a large enough sample to analyze subgroups.

Target outreach to Latinas and Asian women, based on survey data.

Target outreach to oldest women and women who have never been screened.

GOAL 2: Make 50% of women aware that postmenstrual bleeding is a possible symptom of endometrial cancer by 2010.

Evaluate the feasibility of public education about (and ascertain level of knowledge about) endometrial cancer symptoms.

Develop a public education campaign.

GOAL 3: Increase public awareness of ovarian cancer symptoms.

1) Reduce the incidence of late-stage diagnosis by 2010.

Conduct a public education campaign in the District, especially targeted to high-risk women.

 - Develop culturally appropriate information, materials, and training for health care clinics.

 - Develop information, materials, and training for senior citizen centers.

 - Develop information for distribution to health care providers.

2) Improve the amount of accurate staging of ovarian cancer and reduce the
 proportion of cases classified as “stage unknown” to less than 5% by 2010.

Develop physician awareness programs to make community-based primary care physicians, gynecologists, and surgeons aware of the need for appropriate use of gynecologic oncologists.

 


GOAL 4: Improve the quality of care for underinsured and uninsured women in the
District who have gynecologic cancer.

1) Increase information and support to DC clinics and providers treating the target
 population by 2010.

Implement a patient navigation system in clinics for women with gynecologic cancers.

Implement a targeted information campaign to make women eligible for Medicaid benefits aware of and use community services and resources.

Provide continuing professional education for providers operating in District health care clinics.

Encourage gynecologic cancer advocacy groups in the community to provide education and program support in District clinics and cancer centers.

With thanks to Robin Yabroff, PhD, for use of data from prior publications.

 

References for cervical cancer 

Centers for Disease Control and Prevention. Strategies for providing follow-up and treatment services in the National Breast and Cervical Cancer Early Detection Program--United States, 1997. JAMA 1998; 279(24):1941-1942.

Hildesheim A, Gravitt PE, Schiffman MH, Kurman RJ, Barnes WA, Jones S et al. Determinants of genital human papillomavirus infection in low-income women in Washington, D.C. Sex Transm Dis 1993; 20(5):279-285.

Mandelblatt J, Andrews H, Kerner J, Zauber A, Burnett W. Determinants of late stage diagnosis of breast and cervical cancer:
The impact of age, race, social class, and hospital type.
Am J Public Health 1991; 81(5):646-649.

Mandelblatt JS, Lawrence WF, Womack SM, Jacobsen D, Yi B, Hwang Y-T et al. Benefits and costs of using HPV testing to
screen for cervical cancer.
JAMA 2002; 287:2372-2381.

Mitchell JB, McCormack LA. Time trends in late-stage diagnosis of cervical cancer. Differences by race/ethnicity and income.
Med Care 1997; 35(12):1220-1224.

Nanda K, McCrory DC, Myers ER, Bastian LA, Hasselblad V, Hickey JD et al. Accuracy of the Papanicolaou test in screening for and follow-up of cervical cytologic abnormalities: A systematic review. Ann Intern Med 2000; 132(10):810-819.

NCI USDHHS. SEER—Epidemiology and End Results. Bethesda , MD. 2000

Sawaya GF, Brown AD, Washington AE, Garber AM. Current approaches to cervical-cancer screening. N Engl J Med 2001; 344(21):1603-1607.

Schiffman MH. New epidemiology of human papillomavirus infection and cervical neoplasia. J Natl Cancer Inst 1995;
87(18):1345-1347.

Yabroff KR, Mangan P, Mandelblatt JS. Effectiveness of interventions to increase Pap smear use. J Am Board Fam Pract 2003.

References for endometrial (uterine) cancer

American Cancer Society (2005). Cancer Facts and Figures 2005. Atlanta : American Cancer Society.

Ball, H.G., Blessing, J.A., Lentz, S.S., et al. (1996) A phase II trial of paclitaxel in patients with advanced or recurrent
adenocarcinoma of the endometrium: a Gynecologic Oncology Group study.
Gynecol Oncol 62 (2): 278-81.

Burke, T.W., Mundt, A.J., Muggia, F.N. Cancers of the uterine body. In DeVita, V.T., Heilman, S., Rosenberg , S.A. et al. , eds. (2005) Cancer: Principles and Practice of Oncology. Philadelphia : Lippincott Williams & Wilkins, 1341-1359.

Creutzbeerg, C.L., van Putter, W.L., Koper, P.C., et al. (2000) Surgery and postoperative radiotherapy versus surgery alone for patients with stage-1 endometrial carcinoma: multicentre randomized trial. PORTEC Study Group. Post Operative Radiation Therapy in Endometrial Carcinoma. Lancet 355 (9213): 1404-11.

Harris, E.R., Wei, S.J., Chu , C., Acs, G. Cancer of the uterus. In Abeloff, M.D., Armitage, J.O., Lichter, A.S. et al., eds. (2004)
Clinical Oncology. Philadelphia : Elsevier, 2273-2310.

Lentz, SS. (1994) Advanced and recurrent endometrial carcinoma: hormonal therapy. Semin Oncol 21 (1): 100-6.


PDQ Database. Endometrial cancer. Bethesda , MD : National Cancer Institute; 2005. Available at www.cancer.gov. Accessed September 5, 2005.

Rahaman, J., Cohen, C.J., Endometrial cancer. In Kufe, D.W., Pollock, R.E., Weichselbaum, R.R., Bast, R.C. et al, eds. (2003) Cancer Medicine. 6th ed. Hamilton , Ontario : B.C. Decker, 1809-1823.

References for ovarian cancer

Alberts, D.S., Markman, M., Armstrong, D., et al. (2002) Intraperitoneal therapy for stage III ovarian cancer: a therapy whose time has come! J Clin Oncol 20 (19), 3944-6.

American Cancer Society (2005). Cancer Facts and Figures 2005. Atlanta : American Cancer Society

Bookman, M.A. & Young, R.C. (2000). Principles of chemotherapy in gynecologic cancer. In W.J. Hoskins, C.A. Perez, R.C. Young (Eds.) (2000) Principles and Practice of Gynecologic Oncology. Philadelphia : Lippincott Williams & Williams.

Bristow, R.E., Tomacruz, R.S., Armstrong, D.K., et al. (2002) Survival effect of maximal cytoreductive surgery for advanced ovarian carcinoma during the platinum era: a meta-analysis. J Clin Oncol 20 (5), 1248-1259.

Copeland, L.J., Bookman, M., Trimble, E. et al. (2003) Clinical trials of newer regimens for treating ovarian cancer: the rationale for Gyncologic Oncology Group Protocol GOB 182-ICON5. Gynecol Oncol 90 (2Pt 2), S1-7.

Easton , D.F., Ford, D., Bishop, D.T. (1995) Breast and ovarian cancer incidence in BRCA 1-mutation carriers. Breast Cancer
Linkage Consortium.
Am J Hum Genet 56 (1), 265-271.

Goff, B.A., Mandel, L.S., Melancon, C.H., Muntz, H.G. (2004) Frequency of symptoms of ovarian cancer in women presenting
to primary care clinicians.
JAMA 291, 2705-2712.

Markman, M. (2001). Intraperitoneal chemotherapy in the management of malignant disease. Expert Rev Anticancer Ther,
1, 142-148.

Miki, Y., Swensen , J., Shattuck-Eidens, D., et al. (1994). A strong candidate for the breast and ovarian cancer susceptibility gene BRCA 1. Science 266 (5182), 66-71.

Ozols, R.F., Bundy, B.N., Fowler, J., et al. (1999) Randomized phase III study of cisplatin (CIS)/paclitaxel (PAC) versus carboplatin (CARBO)/PAC in optimal stage III epithelial ovarian cancer (OC): a Gynecologic Oncology Group trial (GOG 158). Proceedings of the American Society of Clinical Oncology 18: A-1373, 356a.

Piver, M.S., Goldberg, J.M., Tsukada, Y. et al. (1996) Characteristics of familial ovarian cancer: a report of the first 1,000 families in the Gilda Radner Familial Ovarian Cancer Registry. Eur J Gynaecol Oncol 17 (3), 169-176.

Rubin , S.C. (Ed.) (2004). Chemotherapy of Gynecologic Cancers: Society of Gynecologic Oncologists Handbook 2e. Philadelphia : Lippincott Williams & Wilkins.


Colorectal Cancer

 

Facts in brief:

Text Box: Colorectal cancer, the third most common cancer in the country, is responsible
   for 10% of all cancer deaths. There were an estimated 146,940 new cases
   nationally in 2004 and 56,730 deaths. Among men and women, DC has the
   highest mortality rate from colorectal cancer, higher than the national norm.

The lifetime risk of developing colorectal cancer for both men and women is 6%.
   Americans who die from colorectal cancer lose on average 13.4 years of life.

Since 1985, the incidence of and mortality rate for colorectal cancer has
   been declining about 2% a year, although the decline has been more prominent
   among Whites. The decline is attributed largely to increased screening and
   surveillance and improvements in treatment.

Early detection reduces mortality. Most invasive colorectal cancers begin as polyps, and it takes an average 5 to 15 years before polyps become malignant and form invasive cancers.

The cancer is detected at an early stage, when survival rates are better, among only 27% of White men, 25% of White women, 24% of Black men, and 23% of Black women. For all stages combined, the relative 5-year survival rate is 63% for Whites and 53% for Blacks.

Everyone age 50 or over is at risk and should be screened.

If there is to be only one colonoscopy screening in a lifetime, the most effective age to screen is at 60. Data suggest that screening at this age can reduce mortality from colorectal cancer by 70%. It is better to screen once than not at all.

 


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The burden of colorectal cancer in
Washington , DC

Among U.S. men and women, Washington DC has the highest mortality rate from colorectal cancer, higher (at 25.0 deaths per 100,000 people) than the average U.S. rate (21.2 cases/100,000) (see Table 1). Against a
25-year trend downward in colorectal mortality
rates among Blacks in the U.S. , the past 5 years have seen an increase in colorectal mortality rates in
Blacks in DC..

The annual incidence rate for DC (59.8 cases/
100,000) is higher than the national incidence

 

 

 

 

(53.1 cases/100,000). And the rates of colorectal cancer are higher for Blacks than for Whites in all age groups. In DC, the incidence of colorectal cancer is highest in Wards 2 and 5 and lowest in Ward 3 (see Table 2). Ward 8, despite its high level of poverty, has a relatively low number of cases, perhaps because young people comprise a significant proportion of the ward. For 2005, the estimated number of new cases of colorectal cancer in Washington DC (340) is greater than the estimated number of lung cancer cases (310)—and the number of expected deaths from colorectal cancer in DC is 130.


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Risk factors

Nonmodifiable Risk Factors

Advancing age. Age is the most common risk factor for colorectal cancer. The incidence of the disease increases with age, especially after 60. Thus, screening becomes more effective with age.

Family history of the disease. Most
colorectal cancer is found in people who are not at high risk. But specific mutations have been found in two types of colorectal cancer sometimes inherited in families (see Genetic testing).

Modifiable risk factors

Colonic or rectal polyps. Nearly all colorectal
cancer evolves from adenomas, benign tumors that often grow as a polyp. Polyps are common; when large, they may progress to invasive cancer. But polyps can be both identified and removed through colonoscopy screening. Colonoscopy is required to remove the polyps before they become cancerous. Post-mortem studies show that 25% to 50% of the populationwill have single or multiple adenomas in the colon by age 70.

Inflammatory bowel disease. Inflammatory
bowel disease is associated with a risk for colorectal cancer. Ulcerative colitis that persists for many years may lead to an usually high risk. Crohn’s disease (sometimes called regional ileitis) is also, but infrequently, associated with the cancer.

Inappropriate diet. Studies suggest that obesity is a risk factor for colorectal cancer. Other factors have been implicated, including low consumption of fiber and high consumption of red meat and fat, but these findings have not been substantiated.

Reducing deaths from colorectal cancer

The main interventions to reduce deaths from colorectal cancer include prevention, genetic testing (when

 

 

 

 

 

 

appropriate), screening and early detection of precancerous lesions and cancer.

Primary prevention

Encourage changes in what and how much people eat. Dietary interventions are designed to promote and increase the consumption of foods and nutrients known to reduce the risk of cancer. This means less meat and more fruits, vegetables, and fiber. It also means reducing obesity, a recognized risk factor for colorectal cancer and many other diseases.

Encourage more physical activity. There is evidence that regular physical activity may help prevent the onset of many forms of cancer.

Genetic testing

Encourage genetic testing, when
appropriate.
Individuals
with a family history of colorectal cancer can have their DNA tested to determine whether they have inherited the HNPCC syndrome (hereditary nonpolyposis colorectal cancer) or the FAP (familial adenomatosis polyposis) syndrome, two mutations known to predispose families to colorectal cancer. The HNPCC syndrome often occurs in patients younger than 50, so early testing is advised whenever there is a family history of colorectal cancer.

Screening and early detection

Screening improves the chances of early
detection and the removal of benign
adenomatous polyps (precancerous lesions) and the detection of small, localized cancers that are surgically curable. Unfortunately in DC, two-thirds of colorectal cancers are diagnosed beyond these pre-cancerous or early (localized) stage (see Table 3). The National Cancer
Institute estimates that wide use of screening could save more than 20,000 lives a year.

 


Four screening tests are in common use:
the fecal occult blood test, sigmoidoscopy, colonoscopy, and radiological visualization with double-contrast barium enema. Only the fecal occult blood test can be considered a true screening test because of its reliability, low cost, simplicity, and availability.

Text Box: Early detection reduces
 mortality. Most invasive 
colorectal cancers begin 
as polyps, and it takes
an average 5 to 15 years
 before polyps become 
malignant and form
invasive cancers. Fecal occult blood test (FOBT). The most common screening test for colorectal cancer, FOBT detects small quantities of blood
present in the stool. The test, which can be performed at home, is simple, inexpensive, and available from drug stores. To reduce the risk of cancer, the test should be performed annually for at least 10 years, under a
physician’s guidance.
Because FOBT is a screening test and not a diagnostic test, a positive result should be followed by a colonoscopy. Unfortunately, a high rate of false-positive results greatly increases the number of unnecessary colonoscopies performed. Physicians should inform patients in advance about substances in the diet (such as vitamin C) that can produce
misleading test results.

Sigmoidoscopy. A standard procedure that examines only the distal or left colon and rectum, the sigmoidoscopy is only moderately expensive and takes only a short time. Although sigmoidoscopy is considered effective in reducing deaths from colorectal
cancer, many physicians do not recommend it because it examines only the left side of the colon. If cancer or precancerous lesions are found, colonoscopy must follow.

Colonoscopy. Fiberoptic colonoscopy is
the gold standard in screening, permitting visualization of the inside of the entire colon. Colonoscopy has

 

 

 

 

 

 

 

substantial drawbacks as a screening test. It requires highly trained personnel and is expensive and time-consuming. An intravenous catheter is used to administer sedatives, recovery time is one hour, and a second person must accompany the patient home. But colonoscopy is the only procedure that can identify and remove precancerous polyps and detect early cancer. Colonoscopy should be required of everyone in whom cancer is suspected, who has had previous colorectal cancer, or who is at very high risk. Colonoscopy is most effective in preventing cancer if performed between the ages of 56 and 66, when precancerous polyps are most likely to be present.

Double contrast barium enema. Often used for surveillance by radiologists, this may be useful in some cases for identifying polyps that are difficult to recognize by colonoscopy. Most often, patients are referred by their physician for this procedure.

Follow-up for high-risk patients

Repeated screening at specified intervals is recommended for individuals who are at high risk because of previous polyps, a family
history of the disease, inflammatory bowel disease, or curative-intent resection (surgery) for colorectal cancer. The idea is to detect cancers early so they can be treated before they are able to metastasize. Patients with a history of polyps or surgery for colorectal cancer should undergo regular surveillance, because new polyps or additional primary
cancers often arise in the colon years later.

Barriers to reducing the cancer burden

Screening rates for colorectal cancer remain lower than those for other cancers. Less than



Text Box: half of the U.S. population age 50 and older takes advantage of colorectal cancer tests within the recommended time intervals,
according to a National Health Interview Survey. A successful prevention and control program requires recognizing the barriers to screening for cancer and finding the resources to overcome them—whether they are associated with patients, health care providers,
or the health care system itself. In the final analysis, the most commonly reported
barriers to screening are a lack of awareness about testing and the physician’s failure to recommend testing.

Common barriers as patients see them

The public appears not to have been well informed about the risk of, or the risk factors associated with, colorectal cancer. Despite widespread publicity about colon cancer, increased reimbursement for screening, and data from national health surveys, the screening rates for colorectal cancer are significantly lower than those recorded for breast or cervical cancer. Common reasons
for not undergoing screening include

Practical issues, such as inconvenience
(an entire day is required for a colonoscopy)

Conflicts with work or family

Lack of insurance or medical coverage

Lack of interest

The tests’ unpleasantness

Anxiety about the results

Lack of access

Lack of awareness about testing

Fear of cancer

The idea that cancer cannot be cured

Age (young patients are less compliant
than older patients)

The physician’s failure to recommend
the test.

Barriers among health care providers

The key factor in promoting cancer screening is a physician-patient relationship of trust.
Patients are most likely to comply with
screening if their physician recommends it. One important barrier to screening is the health care providers’ failure to take a careful
family history of cancer and to refer family members for testing if there is evidence of a familial pattern. Other barriers include little or


no access to screening facilities, lack of trained personnel, lack of information about screening
centers, and practice- or capacity-related problems.

Barriers in the health care system

Economics and limited access are barriers
to screening. Reimbursement seems to have
a positive effect on screening rates. The relative odds of Medicare beneficiaries with incomes below $25,000 a year getting a
sigmoidoscopy increased between 1997
and 1999. All groups should be made aware that Medicare provides reimbursement for colonoscopic screening performed every 10 years for patients at average risk.

Rules about reimbursement coverage need to be clarified because lack of knowledge or widespread variation in reimbursement rules and application serve only to discourage screening. Screening should be included in health plans offered by both private and government sources, and reimbursement should not be so low as to discourage screening. Insurers should be made aware that routine screening is cost-effective because it prevents costly treatment and hospitalization.

 


Goals, Objectives, and Strategies

GOAL 1: Reduce the mortality rate in DC from colorectal cancer by 10%.

GOAL 2: Reduce the incidence of invasive disease in DC by 10%.

 

Objectives:

1) Increase to 50% the proportion of colorectal cancer detected at the local stage
 for both men and women by 2010.

2) Increase to 50% the proportion of the adult population that reports having had a
 fecal occult blood test in the previous 2 years by 2010.

3) Increase to 60% the percentage of the population age 50 or older screened by
 sigmoidoscopy or colonoscopy by 2010.

 

Strategies

Encourage professional organizations to promote screening among their members.
Collaborate with DC’s medical societies to promote colorectal cancer prevention and
control and to overcome barriers to screening. Seek representation on the Public Health
and Communications Council of the Medical Society in Washington . Invite professional
medical organizations, especially for primary care, to become active members of the DC
Cancer Coalition.

Develop the infrastructure to provide screening for all DC residents, whatever their cultural
or ethnic background. Do this through collaboration among primary care physicians, internists, surgeons, and gastroenterologists. Create an enduring collaboration that includes public
enterprises, research communities, and professional organizations with an interest in the causes, prevention, and consequences of colorectal cancer.

Develop community education and outreach campaigns about common risk factors and
early symptoms, the benefits of screening and lifestyle modification, centers for screening for all cancers, treatment facilities and support services, and the availability of financial assistance.

Reduce cultural, ethnic, and financial barriers to screening by targeting education programs
to the medically underserved and high-risk populations—taking into account language barriers and low rates of literacy.

Encourage athletes, television personalities, politicians, teachers, and other role models to serve as advocates for routine screening (whatever the test).

Increase the number of physicians who recommend screening to patients and who routinely take a family history of cancer. Train physicians to inquire about every patient’s family history of cancer, whatever the purpose of their medical visit, and invite family members to undergo screening or genetic testing if a familial risk pattern exists. 

 


Encourage physicians to use reminder or other systems for recalling patients for screening.

Make health care professionals aware of centers in DC for colorectal cancer screening and
surveillance, of genetic testing and genetic counseling services, of treatment facilities, and
of cancer rehabilitation centers.

Through professional associations, arrange for scientific presentations, newsletter items,
and postgraduate education about colorectal cancer prevention and control, including the benefits of early detection.

Encourage at least once-in-a-lifetime colonoscopy screening at about 60 as a “rite of
passage.” At least one colonoscopy is better than none, and colonoscopy is most effective
at the age of 60.

Promote better insurance coverage and other forms of assistance for colorectal screening.

 

 

References

Adams EK, Thorpe KE, Becker ER, Joski PP, Flome J. (2004). Colorectal cancer screening, 1997-1999: role of income, insurance and policy. Prevent Med, 38, 551-557.

Anderson WF, Guyton KZ, Hiatt RA, Vernon SW, Levin B, Hawk E. (2002). Colorectal cancer screening for persons at average risk. J Natl Cancer Inst, 94, 1126-1133.

Dunlop MG. (1992). Screening for large bowel neoplasms in individuals with a family history of colorectal cancer. Br J Surg,
79, 488-494.

Lynch HT, Smyrk T. (1996). Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review. Cancer, 78,
1149-1167.

Ramsey SD, Andersen MR, Etzioni R, Moinpour C, Peacock S, Potosky A, Urban N. O. (2000). Quality of life in survivors of
colorectal carcinoma.
Cancer, 88, 1294-1303.

Rawl SM, Menon U, Champion VL, Foster IL, Skinner CS. (2000) Colorectal cancer screening beliefs. Focus groups with
first-degree relatives.
Cancer Pract, 8, 32-37.

Rickert RR, Auerbach O, Garfinkel L, et al. (1979). Adenomatous lesions of the large bowel: an autopsy survey. Cancer, 43,
1847-1857.

Seeff L, Nadel M, Blackman D, and Pollack LA. (2003). Colorectal Cancer Test Use Among Persons Aged 50 Years And
Older–United States , 2001.
Morbidity and Mortality Weekly Report (MMWR), 52, 193–196.

Seeff LC, Nadel MR, Klabunde CN, Thompson T, Shapiro JA, Vernon SW, Coates RJ. (2004). Patterns and predictors of
colorectal cancer test use in the adult U.S. population.
Cancer, 100, 2093-2103.

Sirovich BE, Schwartz LM, Woloshin S. (2003) Screening men for prostate and colorectal cancer in the United States . Does
practice reflect the evidence?
JAMA, 289,11414-1420.

Subramanian S, Klosterman M, Amonkar MM, Hunt TL. (2004). Adherence with colorectal cancer screening guidelines: a review. Prevent Med, 38,536-550.

Walsh JME, Terdiman JP. (2003). Colorectal cancer screening. Scientific Review. JAMA 289.1288-1296.

 

 


Prostate Cancer

 

Facts in brief:

Text Box: Prostate cancer is the second leading cause of cancer deaths among men
   in the U.S. —second only to lung cancer. One in three new cancer cases in men
   arises in the prostate gland.

The projected number of new cases nationally in 2005 is 230,090—with an
   estimated 30,350 men dying from the disease. This is the most commonly
   diagnosed non-skin male cancer in most Western countries.

Estimates are that 610 men in the District will be diagnosed with prostate cancer
   and 80 men will die from the disease in 2005.

The lifetime risk of being diagnosed with invasive prostate cancer is 1 in 6. The
   risk increases from the age of 50 on. Men at higher risk (because they have fathers or
                                               blood-related uncles who had prostate cancer at an early age) should begin testing at age 45.

DC has the highest mortality rate from prostate cancer in the nation. The rate is twice as high in Black men as in White. Incidence rates for Black men in DC are among the highest in the nation. The incidence and death rates for Black men are highest the world over, according to the International Agency for Cancer Research. The risk is lowest in men of Asian descent.

Nationally, the median age for diagnosis is 66 for Black men and 69 for White men. The median age of death from prostate cancer is 77 for Black men and 79 for White.

On average, 9 years of life are lost to prostate cancer.

The causes of prostate cancer are largely unknown.

Prostate cancer eventually affects nearly all men but is clinically unimportant in most men.

 


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An uneven burden

Prostate cancer does not affect everyone equally. Its impact on Black men is
especially hard. As far back as the 1930s, investigators documented racial differences in survival and mortality. The explanations offered today are the same as those offered years ago—including inadequate medical care,
environmental factors, cultural differences, diet, hereditary factors, and social habits.

From 1998 through 2002, there were 2,671 new cases of prostate cancer in the District of Columbia (see Table 1).

 

 

 

 

Incidence and mortality rates (Tables 1 and 2) are highest in Wards 2 and 4. The incidence of prostate cancer in White men began to decline nationally in 1993 and for Black men in 1994. Differences in incidence, clinical stage, and histological (cell) grade are still found in every age group among White and Black men.

Prevention

Currently, there is no known way to prevent prostate cancer, although the National Cancer Institute is conducting research on prevention. Men are usually advised to avoid or minimize risk factors, but this is not always possible.

 

 

 

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Risk factors for prostate cancer

Common risk factors include age, race,
family history of the disease, diet, and serum androgen levels. Nearly all risk factors have been found through studies of White men, so additional risk factors specific to Black men are unknown. Most investigators have assumed that risk factors operate similarly across racial groups.

Age. Age is the strongest risk factor. Prostate cancer is largely a disease of older men; it is rare below the age of 50. The risk increases steadily with age and more than half of all men will have some cancerous growth by the time they are 80, although in most cases it goes unnoticed. Half of all cases are registered in men over 75 and 90% of prostate cancer deaths occur in men 65 and over.

Race. Prostate cancer’s devastating effects
on Black men are reflected in national data. For the years 1998–2002 in DC, the incidence rate of prostate cancer in White men was 160.8 for all ages and 252.1 for Black

 

 

 

men. The mortality rate per 100,000 men was 23.4 for White men and 66.4 for Black.

The onset of invasive prostate cancer comes at a younger age in Black men, and Black men also register premalignant changes earlier. HGPIN (high-grade prostatic intraepithelial neoplasia), a premalignant lesion that progresses to invasive cancer, is more prevalent in Black men than in White. HGPIN was found at autopsy in 18% of Black men in their forties (compared with 14% of White men the same age); in 31% of Black men in their
fifties (21% of White men); in 69% of Black men in their sixties (38% of White men); in 78% of Black men in their seventies (50% of White men); and in 86% of Black men in their eighties (68% of White men). More extensive HGPIN developed earlier in Black men
younger than 60 than in White men the same age. The higher prevalence of HGPIN in Black men may explain the higher incidence of prostate cancer in this population, but
questions remain as to what causes the higher incidence of HGPIN at a relatively young age
in Black men.

Within a clinical setting, Black men are more likely to present with advanced-stage disease and less differentiated tumors than White men. The reason is unknown.

Differences between Black and White men
are evident in many studies. In a military population in which all men have equal access to care, for example, Black men had tumors
averaging two and a half times greater in
volume at diagnosis, had higher mean
(geometric) pretreatment PSA levels, and
were 3 years younger on average than White men. The military setting may eliminate
limitations on access but not necessarily
socioeconomic factors or environmental
differences that affect prostate